Results for "script"

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  • Bioinformatics Codes Search

    ...arrow down your search result. This webpage can be an useful resource for a beginners bioinformatician as it contain several bioinformatics basics script that are commonly used by bio...

    3899 days ago

  • Download mutliple fasta file from NCBI in one GO!!

    ...tract/download all fasta sequences in single click given that you already have a list of GIs or accession IDs . Alternatively, use one liner perl script: perl -ne 'if(/^>(\S+)/){...

    3893 days ago

  • Bioinformatics Scripts

    Some of the useful bioinformatics scripts. For example ... contig-stats.pl is a Perl script that will automatically describe features of a sequence assembly. http://milkweedgenome.org/?q=scripts

    3343 days ago

  • OPERA : Optimal Paired-End Read Assembler

    ...caffolding errors. Furthermore, our latest release contains the wrapper script OPERA-long-read that enables...generation sequencing technologies (PacBio or Oxford Nanopore). The manuscript describing the new features a...

    2778 days ago

  • FERMI

    ....Fermi is designed to be used on a multi-core Linux machine with large shared memory. The easiest way to run fermi is to use the run-fermi.pl script. It generates a Makefile...

    2778 days ago

  • Ribbon !!

    ...e linking the genes CYTH1 and EIF3H. While it has been found in the transcriptome previously, genome sequenc...powerful interactive web tool for viewing complex genomic alignments. Script at https://github.com/Ma...

    2736 days ago

  • R Graphs !!

    The blog is a collection of script examples with example data and output plots. R produce excellent quality graphs for data analysis, science and business presentation, publications and other purposes. Self-help codes and examples are provided. Enjoy nice graphs !!

    2722 days ago

  • Scripts

    Useful script for NGS analysis.

    2695 days ago

  • ScaffMatch

    ...ight Matching able to produce high-quality scaffolds from NGS data (reads and contigs). The tool is written in Python 2.7. It also includes a bash script wrapper that calls aligner in...

    2682 days ago

  • SeqMule: Automated human exome/genome variants detection

    SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can chang...

    2599 days ago