| Projects on Google Code | Results 1 - 10 of 25 |
Project code for Fungal genomics, comparative, and related research at the Stajich lab at UC Riverside.
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==BEDTools Summary==
The BEDTools utilities allow one to address common genomics tasks such as those below, as well as develop sophisticated pipelines that answer complicated research questions.
# Intersecting two BED files in search of overlapping features.
# Merging ove...
TCGA2S3DB is an infrastructure that exposes data from The Cancer Genome Atlas (TCGA) using Semantic Web Formalisms, specifically, as a SPARQL endpoint. Experimental data, such as the one being generated by the TCGA project, is often intrinsically complex and very heterogeneous. For that reason, it ...
A simple library to store and query genomic features and sequence.
* Find neighbors of a given feature up or downstream, or on a given strand.
* Use a feature to slice out sequence from an associated fasta file.
Genedex uses numpy memmaped arrays for fasta slicing of fasta files without creat...
Segway is a segmentation program for functional genomics data.
bioinformatics stuffs. any feedback or contributions would be *greatly* appreciated i can move code to github/bitbucket to facilitate that if it helps:
*NOTE*: as of 2009/10/13 some modules which previously lived here have been moved to [http://bitbucket.org/brentp/biostuff/ bitbucket]
* bio...
bioinformatics,
cython,
bio,
gff,
genomics,
python,
genomic,
fasta,
biology,
randomness,
tests,
genomics
Yet another population genetics toolkit, this time in python.
pgtools is like Rozas' `DNASP`, Thornton's `libsequence`, Cai's `PGEToolbox`, Marchini's `popgen`, but in python.
What it does:
* parses a few of the usual formats, particularly the output of Hudson's `ms`
* computes most of t...
This project includes software and tools to support publication of linked genomic data on the fruit fly (Drosophila).
Sub-projects:
* [Flybase]
* [Bdgp]
* [Flyatlas]
* [Flyted]
We developed a novel mining pipeline, inGAP, which is guided by a Bayesian principle to detect single nucleotide polymorphisms, insertion and deletions by comparing high-throughput pyrosequencing reads with a reference genome of related organisms.
WormBase is the public database for information on C. elegans and related nematodes.