More details are provided within each subfolder.
pileVar.pl identifies variants based on mpileup output from
samtools. This tool is currently geared
toward identifying fixed differences and regions of ambiguity due to indels.
A handful of bioinformatics scripts:
mummer2Vcf.pl
reads file of SNPs and indels called by the Mummer program show-snps -T and produce a VCF-ish file, collapsing consecutive indel characters into a single indel and adding the missing first base from indels by reading from the reference sequence file. The format produced is not yet compliant VCF yet but it will be. Requires BioPerl.
phredDectector.pl
attempts to determine the Phred-scale quality encoding used in a FastQ-format file. If everything looks reasonable, it simply prints 33, 64 or 59 (this last for older Solexa sequences) to stdout. Does not require BioPerl.
fermiExtractContigs.pl
creates Fasta-format contigs from a fermi-format *.fq.gz FastQ-like scaftig files. Writes Fasta to stdout, giving each Fasta sequence its fermi sequence name and a description that includes sequence length, number of non-redundant reads that built the scaftig, and median coverage of non-redundant reads along the scafftig. Requires BioPerl.
fermiExtractContigs_simple.sh
creates Fasta-format contigs from a fermi-format *.fq.gz FastQ-like scaftig files. Unlike fermiExtractContigs.pl, this does not use Perl. Writes Fasta to stdout, giving each Fasta sequence its fermi sequence name and a description that includes sequence length and the number of non-redundant reads that built the scaftig.
windowWig
reads a data stream (for example, coverage values by position within reference sequences) and
produces a USCS WIG file that summarizes median values within nonoverlapping windows.
intervalBed
reads a data stream with reference-position optionally marked with boolean values (for example,
presence-absence by position within reference sequences) and produces a BED file
describing intervals in which the values are true.
samHeader2Bed.pl
reads a SAM header and produces BED file(s) after applying a few filtering criteria.
pileup2pro.pl
reads samtools mpileup format and produces a profile file suitable for input to mlRho.
mergePileupColumns
merges columns from each BAM in multi-BAM samtools mpileup output into single columns.
extractFastaSeqs.pl
extracts named sequences from a FASTA file, or everything but.
shuffleFastq.pl and deshuffleFastq.pl
convert FastQ-format files from separate read 1/read 2 files to interleaved and back. These are based on similar scripts provided with velvet.
fastaGC.pl
analyses GC content of Fasta-format sequences a few different ways.
convertSequence.pland convertAlignment.pl
convert between sequence and alignment formats using BioPerl. If you need to line-wrap a Fasta file, use
convertSequence -f fasta file.fa -of fasta - > outfile.fa
gmhmmp2Fasta.pl and gmhmmp2Table.pl
extract Fasta sequences and a summary table from output produced by the ORF-finding tool gmhmmp.
cutadaptReportScript.sh
collects results from *.cutReport files produced by cutadapt to quicklyl produce a table of adapter trimming results.