Friday, 28 July 2017
Sunday, 5 March 2017
There is currently a problem with the SLiMFinder webserver hosted at UCD, where masking is failing to be performed, regardless of settings. This severely impacts the quality of results. (Disorder, low complexity and n-terminal methionine masking are generally recommended for SLiMFinder.)
I am in communication with the Shields lab to try and get the issue fixed but, until it has been rectified, the bioware.ucd.ie SLiMFinder webserver should not be used.
Friday, 27 January 2017
SLiMSuite species codes are designed to follow the UniprotKB organism (species) identification codes,
using them wherever possible. They form part of the standard
gene_SPECIES__AccNum naming convention for sequences within
SLiMSuite. Species codes should be upper case, and unique for each species.
Tuesday, 11 October 2016
Monday, 12 September 2016
The current SLiMSuite release is
2016-09-12 and can be downloaded by clicking the button (left).
See also: Installation and Setup.
The long-overdue September 2016 release of SLiMSuite
v1.2.0 is now on GitHub. Apart from a few bug fixes, the main updates in this release are to the tools for PacBio genomics, notably
SMRTSCAPE and a new SNP Mapping tool,
Snapper. These are still in development and need further documentation but are ready for use with a little help. Please get in touch if you are interested. Proper documentation and example use will hopefully follow soon, as the first PacBio yeast paper is written.
GABLAM has had some minor tweaks for improved function with
PAGSAT and another developmental tool that will be in the next release (
REVERT - available via the REST servers). These have been focused on the
fragfas=T output of fragmented BLAST hits based on local alignments. This includes addition of a new default to reverse complement reverse hits (
fragrevcomp=T) and the separation of parameters for splitting up local hits into multiple fragments (
gablamfrag=X) and merging close/overlapping fragments (
SLiMSuite updates in this release
Updates in extras/:
• rje_pydocs: Updated from Version 2.16.2.
→ Version 2.16.3: Fixed docstring REST parsing to work with _V* modules.
Updates in libraries/:
• rje: Updated from Version 4.15.1.
→ Version 4.16.0: Added list2dict(inlist,inkeys) and dict2list(indict,inkeys) functions.
→ Version 4.16.1: Improved handling of integer parameters when given bad commands.
→ Version 4.17.0: Added extra functions to randomList()
• rje_blast_V2: Updated from Version 2.9.1.
→ Version 2.10.0: Added nocoverage calculation based on local alignment table.
→ Version 2.11.0: Added localFragFas output method.
→ Version 2.11.1: Fixed snp local table revcomp bug. [Check this!]
→ Version 2.11.2: Fixed GABLAM calculation bug when '*' in protein sequences.
• rje_db: Updated from Version 1.8.0.
→ Version 1.8.1: Added sfdict to saveTable output.
• rje_genbank: Updated from Version 1.3.2.
→ Version 1.4.0: Added addtags=T/F : Add locus_tag identifiers if missing - needed for gene/cds/prot fasta output [False]
→ Version 1.4.1: Fixed genetic code warning.
→ Version 1.5.0: Added setupRefGenome() method based on PAGSAT code.
→ Version 1.5.1: Fixed logskip append locus sequence file bug.
→ Version 1.5.2: Fixed addtag(s) bug.
• rje_hprd: Updated from Version 1.2.
→ Version 1.2.1: Fixed "PROTEIN_ARCHITECTURE" bug.
• rje_menu: Updated from Version 0.3.
→ Version 0.4.0: Changed handling of default for exiting menu loop. May affect behaviour of some existing menus.
• rje_mitab: Updated from Version 0.2.0.
→ Version 0.2.1: Fixed redundant evidence/itype bug (primarily dip)
• rje_obj: Updated from Version 2.1.3.
→ Version 2.2.0: Added screenwrap=X.
→ Version 2.2.1: Improved handling of integer parameters when given bad commands.
• rje_samtools: Updated from Version 0.1.0.
→ Version 0.2.0: Added majmut=T/F : Whether to restrict output and stats to positions with non-reference Major Allele [False]
→ Version 1.0.0: Major reworking. Old version frozen as rje_samtools_V0.
→ Version 1.1.0: Added snptabmap=X,Y alternative SNPTable mapping and read_depth statistics . Added majref=T/F.
→ Version 1.2.0: Added developmental combining of read mapping onto two different genomes.
→ Version 1.3.0: Major debugging and code clean up.
→ Version 1.4.0: Added parsing of read number (to link SNPs) and fixed deletion error at same time. Added rid=T/F and snponly=T/F.
→ Version 1.5.0: Added biallelic=T/F : Whether to restrict SNPs to pure biallelic SNPs (two alleles meeting mincut) [False]
→ Version 1.5.1: Fixed REF/Ref ALT/Alt bug.
→ Version 1.6.0: Added majfocus=T/F : Whether the focus is on Major Alleles (True) or Mutant/Reference Alleles (False) [True]
→ Version 1.7.0: Added parsing of *.sam files for generating RID table.
→ Version 1.8.0: Added read coverage summary/checks.
→ Version 1.8.1: Fixed issue when RID file not generated by pileup parsing. Set RID=True by default to avoid issues.
• rje_samtools_V0: Created/Renamed/moved.
→ Version 0.0: Initial Compilation.
→ Version 0.1.0: Modified version to handle multiple loci per file. (Original was for single bacterial chromosomes.)
→ Version 0.2.0: Added majmut=T/F : Whether to restrict output and stats to positions with non-reference Major Allele [False]
• rje_seq: Updated from Version 3.23.0.
→ Version 3.24.0: Added REST seqout output.
• rje_seqlist: Updated from Version 1.15.3.
→ Version 1.15.4: Fixed REST server output bug.
→ Version 1.15.5: Fixed reformat=fasta default issue introduced from fixing REST output bug.
→ Version 1.16.0: Added edit=T sequence edit mode upon loading (will switch seqmode=list).
→ Version 1.17.0: Added additional summarise=T output for seqmode=db.
→ Version 1.18.0: Added revcomp to reformat options.
→ Version 1.19.0: Added option log description for deleting sequence during edit.
→ Version 1.20.0: Added option to give a file of changes for edit mode.
→ Version 1.20.1: Fixed edit=FILE deletion bug.
• rje_sequence: Updated from Version 2.5.2.
→ Version 2.5.3: Fixed genetic code warning error.
• rje_slimcore: Updated from Version 2.7.5.
→ Version 2.7.6: Added feature masking log info or warning.
→ Version 2.7.7: Switched feature masking OFF by default to give consistent Uniprot versus FASTA behaviour.
• rje_synteny: Created/Renamed/moved.
→ Version 0.0.0: Initial Compilation.
• rje_taxonomy: Updated from Version 1.1.0.
→ Version 1.2.0: Added storage of Parents.
• rje_tree: Updated from Version 2.13.0.
→ Version 2.14.0: Added cladeSpec().
• rje_uniprot: Updated from Version 3.21.4.
→ Version 3.22.0: Tweaked REST table output.
• rje_xref: Updated from Version 1.8.0.
→ Version 1.8.1: Added rest run mode to avoid XRef table output if no gene ID list is given. Added `genes` and `genelist` as `idlist=LIST` synonym.
→ Version 1.8.2: Catching self.dict['Mapping'] error for REST server.
• snp_mapper: Updated from Version 0.4.0.
→ Version 0.5.0: Added CDS rating.
→ Version 0.6.0: Added AltFT mapping mode (map features to AltLocus and AltPos)
→ Version 0.7.0: Added additional fields for processing Snapper output. (Hopefully will still work for SAMTools etc.)
→ Version 0.8.0: Added parsing of GFF file from Prokka.
→ Version 0.8.1: Corrected "intron" classification for first position of features. Updated FTBest defaults.
→ Version 1.0.0: Version that works with Snapper V1.0.0. Not really designed for standalone running any more.
Updates in tools/:
• comparimotif_V3: Updated from Version 3.12.
→ Version 3.13.0: Added REST server function.
• gablam: Updated from Version 2.20.0.
→ Version 2.21.0: Added nocoverage Table output of regions missing from pairwise SNP Table.
→ Version 2.21.1: Added fragrevcomp=T/F : Whether to reverse-complement DNA fragments that are on reverse strand to query [True]
→ Version 2.22.0: Added description to HitSum table.
→ Version 2.22.1: Added localaln=T/F to keep local alignment sequences in the BLAST local Table.
→ Version 2.22.2: Fixed local output error. (Query/Qry issue - need to fix this and make consistent!)
→ Version 2.22.3: Fixed blastv and blastb error: limit also applies to individual pairwise hits!
→ Version 2.23.0: Divided GablamFrag and FragMerge.
• pagsat: Updated from Version 1.6.1.
→ Version 1.7.0: Added tidy=T/F option. (Development)
→ Version 1.7.1: Updated tidy=T/F to include initial assembly.
→ Version 1.7.2: Fixed some bugs introduced by changing gablam fragment output.
→ Version 1.7.3: Added circularise sequence generation.
→ Version 1.8.0: Added orphan processing and non-chr naming of Reference.
→ Version 1.9.0: Modified the join sorting and merging. Added better tracking of positions when trimming.
→ Version 1.9.1: Added joinmargin=X : Number of extra bases allowed to still be considered an end local BLAST hit 
→ Version 1.10.0: Added weighted tree output and removed report warning.
→ Version 1.10.1: Fixed issue related to having Description in GABLAM HitSum tables.
→ Version 1.10.2: Tweaked haploid core output.
→ Version 1.10.3: Fixed tidy bug for RevComp contigs and switched joinsort default to Identity. (Needs testing.)
→ Version 1.10.4: Added genetar option to tidy out genesummary and protsummary output. Incorporated rje_synteny.
→ Version 1.10.5: Set gablamfrag=1 for gene/protein hits.
→ Version 1.11.0: Consolidated automated tidy mode and cleaned up some excess code.
→ Version 1.11.1: Added option for running self-PAGSAT of ctidX contigs versus haploid set. Replaced ctid "X" with "N".
→ Version 1.11.2: Fixed Snapper run choice bug.
• pingu_V4: Updated from Version 4.5.3.
→ Version 4.6.0: Added hubonly=T/F : Whether to restrict pairwise PPI to those with both hub and spoke in hublist [False]
→ Version 4.6.1: Fixed some ppifas=T/F bugs and added combineppi=T/F : Whether to combine all spokes into a single fasta file [False]
→ Version 4.6.2: Added check/filter for multiple SpokeUni pointing to same sequence. (Compilation redundancy mapping failure!)
→ Version 4.6.3: Fixed issue with 1:many SpokeUni:Spoke mappings messing up XHub.
→ Version 4.7.0: Added ppidbreport=T/F : Summary output for PPI compilation of evidence/PPIType/DB overlaps [True]
→ Version 4.8.0: Fixed report duplication issue and added additional summary output
• qslimfinder: Updated from Version 2.1.0.
→ Version 2.1.1: Switched feature masking OFF by default to give consistent Uniprot versus FASTA behaviour.
• seqsuite: Updated from Version 1.11.0.
→ Version 1.11.1: Redirected PacBio to call SMRTSCAPE.
→ Version 1.11.2: Fixed batchrun batchlog=False log error.
→ Version 1.12.0: Added Snapper.
• slimfarmer: Updated from Version 1.4.3.
→ Version 1.4.4: Modified default vmem request to 126GB from 127GB.
→ Version 1.4.5: Updated BLAST loading default to 2.2.31
• slimfinder: Updated from Version 5.2.1.
→ Version 5.2.2: Added warnings for ambocc and minocc that exceed the absolute minima. Updated docstring.
→ Version 5.2.3: Switched feature masking OFF by default to give consistent Uniprot versus FASTA behaviour. Fixed FTMask=T/F bug.
• slimparser: Updated from Version 0.3.3.
→ Version 0.3.4: Tweaked error messages.
→ Version 0.4.0: Added simple json format output.
• slimprob: Updated from Version 2.2.4.
→ Version 2.2.5: Fixed FTMask=T/F bug.
• slimsearch: Updated from Version 1.7.
→ Version 1.7.1: Minor modification to docstring. Preparation for update to SLiMSearch 2.0 optimised for proteome searches.
• slimsuite: Updated from Version 1.5.1.
→ Version 1.5.2: Updated XRef REST call.
→ Version 1.6.0: Removed SLiMCore as default. Default will now show help.
• smrtscape: Updated from Version 1.8.0.
→ Version 1.9.0: Updated empirical preassembly mapefficiency calculation.
→ Version 1.10.0: Added batch processing of subread files.
→ Version 1.10.1: Fixed bug in batch processing.
• snapper: Created/Renamed/moved.
→ Version 0.0.0: Initial Compilation.
→ Version 0.1.0: Tidied up with improved run pickup.
→ Version 0.2.0: Added FASTQ and improved CNV output along with all features.
→ Version 0.2.1: Fixed local output error. (Query/Qry issue - need to fix this and make consistent!) Fixed snp local table revcomp bug.
→ Version 0.2.2: Corrected excess CNV table output (accnum AND shortname).
→ Version 0.2.3: Corrected "intron" classification for first position of features. Updated FTBest defaults.
→ Version 1.0.0: Working version with completed draft manual. Added to SeqSuite.
→ Version 1.0.1: Fixed issues when features missing.
Tuesday, 23 August 2016
SMRTSCAPE (SMRT Subread Coverage & Assembly Parameter Estimator) is tool in development as part of our PacBio sequencing projects for predicting and/or assessing the quantity and quality of useable data required/produced for HGAP3 de novo whole genome assembly. The current documentation is below. Some tutorials will be developed in the future - in the meantime, please get in touch if you want to use it and anything isn’t clear.
The main functions of
Estimate Genome Coverage and required numbers of SMRT cells given predicted read outputs. NOTE: Default settings for SMRT cell output are not reliable and you should speak to your sequencing provider for up-to-date figures in their hands.
Summarise the amount of sequence data obtained from one or more SMRT cells, including unique coverage (one read per ZMW).
Calculate predicted coverage from subread data for difference length and quality cutoffs.
Predict HGAP3 length and quality settings to achieve a given coverage and accuracy.
SMRTSCAPE will be available in the next SLiMSuite download. The
coverage=T mode can be run from the EdwardsLab server at: http://www.slimsuite.unsw.edu.au/servers/pacbio.php. (This is currently running a slightly old implementation but should be updated shortly.)
Version: 1.10.1 Last Edit: 26/05/16
### ~ General Options ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ### genomesize=X : Genome size (bp)  ### ~ Genome Coverage Options ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ### coverage=T/F : Whether to generate coverage report [False] avread=X : Average read length (bp)  smrtreads=X : Average assemble output of a SMRT cell  smrtunits=X : Units for smrtreads=X (reads/Gb/Mb) [reads] errperbase=X : Error-rate per base [0.14] maxcov=X : Maximmum X coverage to calculate  bysmrt=T/F : Whether to output estimated coverage by SMRT cell rather than X coverage [False] xnlist=LIST : Additional columns giving % sites with coverage >= Xn [1+`minanchorx`->`targetxcov`+`minanchorx`] ### ~ SubRead Summary Options ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ### summarise=T/F : Generate subread summary statistics including ZMW summary data [False] seqin=FILE : Subread sequence file for analysis [None] batch=FILELIST : Batch input of multiple subread fasta files (wildcards allowed) if seqin=None  targetcov=X : Target percentage coverage for final genome [99.999] targeterr=X : Target errors per base for preassembly [1/genome size] calculate=T/F : Calculate X coverage and target X coverage for given seed, anchor + RQ combinations [False] minanchorx=X : Minimum X coverage for anchor subreads  minreadlen=X : Absolute minimum read length for calculations (use minlen=X to affect summary also)  rq=X,Y : Minimum (X) and maximum (Y) values for read quality cutoffs [0.8,0.9] rqstep=X : Size of RQ jumps for calculation (min 0.001) [0.01] ### ~ Preassembly Fragmentation analysis Options ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ### preassembly=FILE: Preassembly fasta file to assess/correct over-fragmentation (use seqin=FILE for subreads) [None] ### ~ Assembly Parameter Options ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ### parameters=T/F : Whether to output predicted "best" set of parameters [False] targetxcov=X : Target 100% X Coverage for pre-assembly  xmargin=X : "Safety margin" inflation of X coverage  mapefficiency=X : [Adv.] Efficiency of mapping anchor subreads onto seed reads for correction [1.0] xsteplen=X : [Adv.] Size (bp) of increasing coverage steps for calculating required depths of coverage [1e6] parseparam=FILES: Parse parameter settings from 1+ assembly runs  paramlist=LIST : List of parameters to retain for parseparam output (file or comma separated, blank=all)  predict=T/F : Whether to add XCoverage prediction and efficiency estimation from parameters and subreads [False] ### ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ ###
SMRTSCAPE has a number of functions for PacBio sequencing projects, concerned with predicting and/or assessing the quantity and quality of useable data produced:
- Summarise subreads (
summarise=T). This function summarises subread data from a given
seqin=FILEfasta file, or a set of subread fasta files given with
- Calculate length cutoffs (
calculate=T). Calculates length cutoffs for different XCoverage combinations from subread summary data.
- Parameters (
parameters=T). This function attempts to generate predicted optimum assembly settings from the
- Genome Coverage (
coverage=T). This method tries to predict genome coverage and accuracy for different depths of PacBio sequencing.
- Preassembly fragmentation analysis (
- Parse Parameters (
parseparam=FILES). This method parses assembly parameters from the SmrtPipeSettings Summary file.
- Prediction (
predict=T). This method compares predicted coverage from seed reads with estimated coverage from preassembly data.
These are explored in more detail below.
The setup phase primarily sorts out the
SMRTSCAPE objects. With the exception of pure
ParseParam runs, it will also set up:
- Genome Size. Unless given with
genomesize=X, this will be asked for as it is required X coverage/depth and accuracy calculations.
- Target Error Rate. Unless given with
targeterr=X, a target error rate of 1/
GenomeSizewill be set.
- Basefile. Finally, if no
basefile=Xsetting is given, the basename for output files will be set to the basename of
seqin=FILEif given (stripping
.subreadsif present), else
Summarise subreads (summarise=T)
This function summarises subread data from a given
seqin=FILE fasta file, or a set of subread fasta files given with
batch=FILELIST. This uses the
summarise=T function of
rje_seqlist to first give text output to the log file of some summary statistics:
- Total number of sequences.
- Total length of sequences.
- Min. length of sequences.
- Max. length of sequences.
- Mean length of sequences.
- Median length of sequences.
- N50 length of sequences.
Next, Pacbio-specific subread header information will be parsed to generate three summary tables (described in more detail below):
*.zmw.tdtsummary of all subreads.
*.unique.tdtsummary of the longest subread per ZMW.
*.rq.tdtsummary of subread data for different Read Quality values.
These are generated by parsing both the sequence data and the sequence name data:
>m150625_001530_42272_c100792502550000001823157609091582_s1_p0/9/0_3967 RQ=0.784 >m150625_001530_42272_c100792502550000001823157609091582_s1_p0/11/0_20195 RQ=0.868
These are split into component parts:
m150625_001530_42272_c100792502550000001823157609091582_s1_p0= SMRT cell (
/9= ZMW (
/0_3967= raw read positions used for subread (5’ adaptor removed) (
RQ=0.784= read quality (mean per base accuracy) (
The numbers and “best” subreads for each ZMW are summarised in
#RN log file entries.
Subread output (*.zmw.tdt)
The first output file is the
*.zmw.tdt, which stores the subread information:
RQ= as above.
RN= subread number within ZMW (1 to N).
Len= length of subread.
Seq= sequence file position.
The unique key for this file is:
Unique subread output (*.unique.tdt)
This table is made from
*.zmw.tdt by reducing each ZMW’s output to a single read. Reads are kept in preference of (a) longest, (b) read quality (if tied), and finally (c) earliest read (if tied for both). It hase the same fields as
*.zmw.tdt with keys determined by:
Read Quality output (*.rq.tdt)
This table outputs the number and percentage of subreads and longest reads at each read quality (
RQ= read quality (per base accuracy)
xerr= the Xdepth required @ that
RQto meet the
targeterr=Xerror per base accuracy.
subread= number of subreads with that
unique= number of “best” unique subread per ZMW with that
f.subreads= proportion of subreads with that
f.unique= proportion of unique subreads with that
cum.subreads= proportion of subreads with quality >=
cum.unique= proportion of unique subreads with quality >=
x.subreads= XCoverage of subreads with quality >=
x.unique= XCoverage of unqiue subreads with quality >=
MeanRQ= mean read quality of bases in subreads with quality >=
Mean.XErr= the Xdepth required at that
MeanRQto meet the
targeterr=Xerror per base accuracy.
Calculate length cutoffs (calculate=T)
This function calculates length cutoffs for different XCoverage combinations from subread summary data. It uses the
*.rq.tdt files from above, generating if required (and regenerating if
XCovLimit data are calculated. These are the summed read lengths required to generate the desired genome coverage (
targetcov=X) at different depths of X coverage. Note that the square root of the
targetcov=X value is used, as the HGAP assembly process involves two layers of genome coverage: (1) coverage of seed reads by anchor reads to generate the pre-assembly; (2) coverage of the pre-assembly.
XCovLimit data are calculated by incrementing total summed read lengths in 1 Mb increments (adjusted with
xsteplen=X). At each incremment,
genomesize=X is used to calculate the total X coverage. The probability of the target
X coverage (starting at
1X) given the total X coverage is then calculated using a Poisson distribution. If this probability exceeds the target genome coverage, the current summed length is set as the
X and the target
X increased by 1. The total summed read length is then incremented by
xsteplen and the process repeated until the summed length reaches the total length of all subreads of at least the size set by
minreadlen=X (default 500 bp).
Next, the read quality steps to calculate are established using
rq=X,Y (minimum (
X) and maximum (
Y) read quality cutoffs, defaults=0.8-0.9) and
rqstep=X (the size of
RQ steps for calculations, default=0.01 (min 0.001).
Finally, the seed and anchor lengths required to achieve certain minimum Xdepths of target genome coverage are calculated and output to
TargetErr is used to establish the min. required anchor read Xdepth (
AnchorMinX). If this exceeds the specified
minanchorx=X value, this will be used as the minimum target instead. Next, the seed read length (
SeedLen) required to get a combined unique seed read length to give a minimum Xdepth (
targetxcov=X is calculated. Where
xmargin > 0, additional seed lengths will also be calculated to give deeper minimum seed Xdepths. e.g.
targetxcov=3 xmargin=2 will calculate
5X. For each
SeedLen, anchor read length cutoffs are also calculated such that the summed length of unique reads where
AnchorLen <= length <
SeedLen is sufficent to give
AnchorMinX values from the minimum established above until
XMargin is reached.
If there is insufficient data to meet the minimum seed and anchor read depths, the “optimal” seed XCoverage will be calculated from the unique seed reads, as described for
coverage=T. In essence,
SeedMinX will be reduced to meet
AnchorMinX until it falls below zero and then the two values will be optimised to try and maximise genome coverage at the required target error. Users may prefer instead to relax the
minanchorx=X values. This optimisation is based on unique Xcoverage and the precise values subsequently output in
*.cutoffs.tdt may differ. (Relaxed variations could be run with higher
xmargin=X values to output a range from which the chosen values can be selected for
mapefficiency=X is used during this process to reduce the effective seed coverage at a given summed length and thus inflate the required
SeedX needed to achieve a given
This table contains the main output from the
calculate=T function. Unique entries are determined by combinations of
RQ= Read Quality Cutoff.
SeedMinX= Min seed XCoverage for TargetCov % of genome (unique reads). If this is <1, it indicates the proportion of the genome covered at 1X.
SeedLen= Seed length Cutoff.
SeedX= Total Seed read XCoverage (all reads).
AnchorMinX= Min anchor XCoverage for TargetCov % of genome (unique reads). If this is <
minanchorx=X, it indicates the proportion of the genome covered at
AnchorLen= Anchor read (i.e. overall subread) length cutoff.
AnchorX= Total Anchor read XCoverage (all reads).
Preassembly fragmentation analysis (preassembly=FILE)
[ ] : Add preassembly details here.
Optimal Assembly Parameters (parameters=T)
parameters=T function attempts to generate predicted optimum assembly settings from the
calculate=T table data.
*.cutoffs.tdttable is read in (or generated if required).
xmargin=Xsettings are used to determine the desired
SeedMinXvalue, i.e. the miniumum depth of coverage of the chosen seed reads. (NB. The
mapefficiency=Xsetting is used for inflating the required XCoverage needed to meet this Min XDepth during the calculate process.)
- Each potential
RQcutoff is now assessed and the
targeterr=Xsetting used to determine the required Xdepth per base for error correction. Note: This uses the minimum RQ value and should thus be conservative. Using the mean RQ was considered but it was deemed that conservative is best in this scenario.
- The desired
AnchorMinXis calculated from the target Xdepth and
xmargin=X. The final value is reduced by one to allow for the fact that the seed read counts as X=1 for error estimation.
- Parameter combinations have now been reduced to those with the desired Seed and Anchor minimum Xdepth. Two parameter combinations are then output:
- MaxLen parameters using the mininum RQ value and thus the longest seed and anchor read length cutoffs.
- MaxRQ parameters using the maximum RQ value.
Note that the predicted parameter settings are only output as
#PARAM log entries: the full set (including these “optimal” ones) are part of the
Genome Coverage (coverage=T)
This method tries to predict genome coverage and accuracy for different depths of PacBio sequencing based on predicted usable output statistics and the genome size. Statistics for existing runs can be generated using the
summarise=T option and used to inform
calculate=T if run together.
Setup. If the
summarise=T option is used and/or there is an existing
BASEFILE.unique.tdt file (and
force=F) then the
*.unique.tdt table will be used to generate SMRT cells statistics: mean read count (used to populate
smrtreads=X); mean total read count (used to populate
avread=X); mean RQ (used to populated
errperbase=X). Otherwise, the corresponding commandline options will be used. If
smrtreads=X will be recalculated as
XnList. The second stage of setup is to calculate the %coverage at certain X depth coverage to be calculated along with overall depth of coverage etc. These numbers are based on the subread
minanchorx. Any levels explicitly chosen by
xnlist=LIST will also be calculated.
TargetXDepth. Next, target Xdepth values are calculated in the same fashion as
XCovLimit data (above), except that these are now converted to Xcoverage (based on
GenomeSize) rather than total subread lengths.
Accuracy. The % genome coverage and accuracy for different X coverage of a genome are then calculated assuming a non-biased error distribution. Calculations use binomial/poisson distributions, assuming independence of sites. Accuracy is based on a majority reads covering a particular base with the correct call, assuming random calls at the other positions (i.e. the correct bases have to exceed 33% of the incorrect positions). The
errperbase=X parameter is used for this calculation.
Coverage. Coverage statistics are then calculated for each Xdepth of sequencing (or SMRT cell if
bysmrt=T) First, the optimal seed read Xcoverage is calculated. The target seed Xdepth (
targetxcov=X) and anchor depth (
minanchorx=X) are used to identify the total target Xcoverage. If this is met (inflating required seed coverage to account for
mapefficiency=X), the largest seedX value that meets the
minanchorx=X anchor depth is selected. If this cannot be achieved with seedX >= 1, the optimal balance between seed length and anchor length is achieved by maximising the probability of 1X seed coverage and
MinAnchorX+ anchor coverage. This seed read length is then used to generate the predicted coverage output.
Main output is the
*.coverage.tdt file. All calculations are based on subreads, and therefore using the “raw” polymerase read data for the
smrtreads=X value for SMRT cells will overestimate coverage. Note that
smrtreads=X can be used to input sequence capacity in Gb (or Mb) rather than read counts by changing
XCoverage= Total mean depth of coverage.
SMRT= Total number of SMRT cells.
%Coverage= Estimated %coverage of assembly.
%Accuracy= Estimated %accuracy of assembled genome. This is established by working out the predicted proportion of the genome at each Xcoverage (given the total
XCoverage) and the accuracy at that depth (as described above).
%Complete= Product of %coverage and %accuracy.
SeedX= Estimated optimal depth of coverage for seed reads.
Parsing assembly parameters (ParseParam=FILES)
This method will take a bunch of
*.settings text files (wildcards allowed) and parse out the assembly parameter settings into a delimited text file. The contents of these files should be consistent with the
Assembly_Metrics_*.xlsx file produced by the SMRT Portal.
Output for this method is a
*.settings.tdt file, which has the following field headers:
Setting. The full setting name, e.g.
Prefix. The setting prefix, e.g.
Suffix. The setting suffix, e.g.
minCorCov. (This is used for some of the
Variable. Whether the parameter is variable (“TRUE”) or fixed (“FALSE”) in the set of
*.settingsfiles being parsed.
Assemblies. Each assembly (the
*.settings) will get its own field containing the actual value used for that parameter in that assembly.
NOTE: The files coming off SMRT Portal have some undesirable non-unicode characters in them. These are hopefully stripped by
SMRTSCAPE but it is possible that some parameters may not be correctly parsed.
It is possible to parse a selected subset of parameters using
paramlist=LIST. (This is easiest where
LIST is a text file with one parameter per line.) This should be a list of the full parameter name, i.e. the content of the
[ ] : Add the recommended list of parameters here.
Predicting assembly coverage (Predict=T)
This function predicts coverage from parsed assembly parameters and compares to pre-assembly subreads if possible. Its primary function is to check that the parameter settings from
calculate=T are working as expected (at least in terms of preassembly generation) and to tweak the
mapefficiency=X option if required. Where a reference is available, it can also be used to test the make
SRMTSCAPE calculations in terms of coverage etc.
Predict uses data from the
parseparam=FILES functions. (These will be run if required.) As such, it requires the original subread data (
seqin=FILE) and the list of
*.settings files that identifies the assemblies. (See
*.preassembly.fasta files should match the
*.settings files. (The file looked for will be identified as a
#PREX log entry.)
If it already exists, the
*.predict.tdt will be loaded and updated. Otherwise a new
*.predict.tdt file will be created. (See below.)
Predict first loads in the relevant data and assembly parameters (see output) before calculating expected coverage from subread data and observed coverage from preassembly data.
The output of
Predict mode is a
*.predict.tdt output file with the following fields:
Assembly= The assembly base filename for a given file in
SeedX= mean depth of coverage for seed reads given seed length and min RQ score.
AnchorX= mean depth of coverage for anchor reads given seed length and min RQ score.
SeedMinX= minimum depth of coverage of unique seed reads to achieve
AnchorMinX= minimum depth of coverage of unique anchor reads to achieve
PreCov= predicted base coverage of pre-assembly.
CorPreCov= corrected predicted base coverage of pre-assembly given
PreX= average depth of coverage of
PreMinX= minimum depth of coverage of
*.preassembly.fastasequences to achieve
SeedXas an estimate of the loss of seed sequence during the preassembly mapping phase. Ideally, this should be close to the
mapefficiency=Xsetting. (NOTE: SMRTSCAPE has not undergone extensive testing of this assumption.