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Galaxy Bioinformatics Platform

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  Analyzed 3 months ago

Galaxy allows you to do analyses you cannot do anywhere else without the need to install or download anything. You can analyze multiple alignments, compare genomic annotations, profile metagenomic samples and much much more... We provide a public Galaxy instance at https://usegalaxy.org where you ... [More] can do all this with nothing more than a web browser. [Less]

1.86M lines of code

164 current contributors

4 months since last commit

12 users on Open Hub

Activity Not Available
5.0
 
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SNAP-aligner

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  Analyzed 3 months ago

Scalable Nucleotide Alignment Program -- a fast and accurate read aligner for high-throughput sequencing data

49.4K lines of code

4 current contributors

about 2 years since last commit

2 users on Open Hub

Activity Not Available
5.0
 
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Licenses: No declared licenses

Blat-like Fast Accurate Search Tool

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  No analysis available

BFAST facilitates the fast and accurate mapping of short reads to reference sequences, where mapping billions of short reads with variants is of utmost importance.

0 lines of code

0 current contributors

0 since last commit

0 users on Open Hub

Activity Not Available
0.0
 
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Mostly written in language not available
Licenses: No declared licenses

Orione tools

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  Analyzed 3 months ago

Collection of tools used by http://orione.crs4.it

13.2K lines of code

0 current contributors

over 7 years since last commit

0 users on Open Hub

Activity Not Available
0.0
 
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ngs

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  Analyzed 3 months ago

Next generation sequencing (NGS/HTS) tools.

32.6K lines of code

0 current contributors

almost 5 years since last commit

0 users on Open Hub

Activity Not Available
0.0
 
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