WhopGenome
0.9.7High-Speed Processing of VCF, FASTA and Alignment Data
Overview
Provides very fast access to whole genome, population scale variation data from VCF files and sequence data from FASTA-formatted files. It also reads in alignments from FASTA, Phylip, MAF and other file formats. Provides easy-to-use interfaces to genome annotation from UCSC and Bioconductor and gene ontology data from AmiGO and is capable to read, modify and write PLINK .PED-format pedigree files.
Install
Health
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Documentation
- Examples that run
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- Documented parameters
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- Return-value docs
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- References docs
- 2%
Downloads
Dependencies
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Code & Tests
People & History
11 releases. Pick two to compare their code metrics. R releases are shown for context.
- RR 4.0.0 released · 2020-04-24
- archivedRemoved from CRAN2020-03-03check problems were not corrected despite reminders
- RR 3.6.0 released · 2019-04-26
- RR 3.5.0 released · 2018-04-23
- RR 3.4.0 released · 2017-04-21
- 0.9.72017-03-13 · diff ↗
- 0.9.62017-03-02 · diff ↗
- 0.9.42016-07-07 · diff ↗
- RR 3.3.0 released · 2016-05-03
- 0.9.32015-09-08 · diff ↗
- RR 3.2.0 released · 2015-04-16
- 0.9.22015-02-17 · diff ↗
- 0.9.12015-02-17 · diff ↗
- 0.9.02014-07-07 · diff ↗
- 0.8.92014-07-07 · diff ↗
- RR 3.1.0 released · 2014-04-10
Package metadata
- Total releases
- 11
- License
- GPL (>= 2) OSI
- Minimum R
- ≥ 1.8.0
- Download size
- not tracked yet
- Installed size
- not tracked yet
- With dependencies
- not tracked yet
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