| Script Description |
|
assemblathon_stats.pl
|
Extracts the assembly stats of a genome fasta file |
| batch_genscan.pl |
Run the genscan gene prediction program in batch mode. Runs genscan as well as converts output to gff format |
| extract_region.pl |
Given a fasta and a coordinates file extracts the region corresponding to the coordinates |
| fastq2fasta.pl |
Converts a fastq to fasta file |
| filterByLength.py |
Filters a multifasta format file based on a length cutoff |
| genomeLength.py |
Provides the lengths of chromosome as well as the total genome size |
| getReadLengths.py |
Provides the lengths of the reads in a fastq file |
| gff2gtf.py |
Converts gff format to the gtf file |
| NCBI_retrieval.pl |
Retrieves the sequences (EST seq., unigenes, gene seq, books etc) from NCBI repository |
| seqtk |
Post processing and format conversions of fasta/Fastq files |
| splitfasta.py |
Split a multi fasta format file into individual fasta sequence files |
| vcfutils.pl |
Format conversions and filtering of the vcf files |
| renamefq.py |
Rename headers of a fastq file |
| extract_flanking_regions.pl |
Extracts the regions of a fasta file with flanking regions from an assembly fasta file |
| ISMU_v1.0.tar.gz |
ISMU pipeline http://hpc.icrisat.cgiar.org/ISMU/ |