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samtools
S
Analyzed about 20 hours ago
SAM (Sequence Alignment/Map) is a flexible generic format for storing nucleotide sequence alignment. SAM tools provide efficient utilities on manipulating alignments in the SAM format.
Licenses:
mit
pysam
P
Analyzed about 7 hours ago
Pysam is a python module for reading and manipulating Samfiles. It's a lightweight wrapper of the samtools C-API. Pysam also includes an interface for tabix.
Exome Variant Analysis
No analysis available
Exome Variant Analysis Pipeline (NGS Data). Developed in R language, calling external programs for specific tasks. It can be run in parallel using many processors from the same machine, and can be easily extended to run in computer clusters (HPC). Still in its early stages, it's a work in progress
Mostly written in language not available
Licenses:
ccbysa3-0, lgpv3_or_...
MiModD
Analyzed about 17 hours ago
MiModD is an integrated solution for mapping-by-sequencing analysis of whole-genome sequencing (WGS) data from laboratory model organisms. It enables geneticists to identify the genetic mutations present in an organism starting from just raw WGS read data and a reference genome without the help of a
cufflinks
C
Analyzed about 10 hours ago
Cufflinks assembles transcripts, estimates their abundances, and tests for differential expression and regulation in RNA-Seq samples. It accepts aligned RNA-Seq reads and assembles the alignments into a parsimonious set of transcripts. Cufflinks then estimates the relative abundances of these
vidjil
V
Analyzed about 17 hours ago
Vidjil is an open-source platform for the analysis of high-throughput sequencing data from lymphocytes, developed by the Bonsai bioinformatics team and its collaborators. V(D)J recombinations in lymphocytes are essential for immunological diversity. They are also useful markers of pathologies, and