r-goalie
|
public |
Assertive check functions for defensive R programming.
|
2024-12-12 |
cofold
|
public |
An RNA secondary structure prediction method that takes co-transcriptional folding into account.
|
2024-12-12 |
nmrglue
|
public |
A module for working with NMR data in Python
|
2024-12-12 |
maxit
|
public |
MAXIT assists in the processing and curation of macromolecular structure data.
|
2024-12-12 |
abpoa
|
public |
abPOA: fast SIMD-based partial order alignment using adaptive band
|
2024-12-12 |
trf
|
public |
Tandem Repeats Finder is a program to locate and display tandem repeats in DNA sequences.
|
2024-12-12 |
ucsc-countchars
|
public |
Count the number of occurrences of a particular char
|
2024-12-12 |
vcftools
|
public |
A set of tools written in Perl and C++ for working with VCF files. This package only contains the C++ libraries whereas the package perl-vcftools-vcf contains the perl libraries
|
2024-12-12 |
seqtk
|
public |
Seqtk is a fast and lightweight tool for processing sequences in the FASTA or FASTQ format
|
2024-12-12 |
ninja-nj
|
public |
Nearly Infinite Neighbor Joining Application
|
2024-12-12 |
scssim
|
public |
A bioinformatics tool for simulating single-cell genome sequencing data
|
2024-12-12 |
ucsc-wordline
|
public |
chop up words by white space and output them with one
|
2024-12-12 |
sdust
|
public |
Symmetric DUST for finding low-complexity regions in DNA sequences.
|
2024-12-12 |
haploflow
|
public |
Strain-aware viral genome assembler for short read sequence data
|
2024-12-12 |
mapcaller
|
public |
MapCaller: combined short-read mapper and variant caller
|
2024-12-12 |
ucsc-netsplit
|
public |
Split a genome net file into chromosome net files
|
2024-12-12 |
ucsc-qacagplift
|
public |
Use AGP to combine per-scaffold qac into per-chrom qac.
|
2024-12-12 |
mergenotcombined
|
public |
Merge Forward and reverse reads from fastq files
|
2024-12-12 |
bamhash
|
public |
No Summary
|
2024-12-12 |
ucsc-faalign
|
public |
Align two fasta files
|
2024-12-12 |
evidencemodeler
|
public |
Evidence Modeler combines ab intio gene predictions, protein alignments, and transcript alignments into weighted consensus gene structures
|
2024-12-12 |
booster
|
public |
BOOSTER is a new way of computing bootstrap supports in large phylogenies.
|
2024-12-12 |
rustynuc
|
public |
Quick analysis of pileups for likely 8-oxoG locations
|
2024-12-12 |
assemblyutility
|
public |
No Summary
|
2024-12-12 |
smoothxg
|
public |
Local reconstruction of variation graphs using partial order alignment
|
2024-12-12 |
vcfbub
|
public |
Popping bubbles in vg deconstruct VCFs
|
2024-12-12 |
ucsc-pslsortacc
|
public |
Remove chain-breaking alignments from chains that break nested chains.
|
2024-12-12 |
python-hyphy-python
|
public |
HyPhy package interface library
|
2024-12-12 |
fastsimbac
|
public |
Models bacterial recombination
|
2024-12-12 |
selam
|
public |
Simulation of Epistasis Local adaptation, with Ancestry and Mate choice
|
2024-12-12 |
ucsc-catdir
|
public |
concatenate files in directory to stdout.
|
2024-12-12 |
ucsc-fatotab
|
public |
convert fa file to tab separated file
|
2024-12-12 |
ucsc-getrnapred
|
public |
Get virtual RNA for gene predictions
|
2024-12-12 |
aprfinder
|
public |
Tool for finding aphased repeats.
|
2024-12-12 |
r-loom
|
public |
An interface for the single-cell RNAseq-oriented loom format. Loom files are an HDF5-based format for storing and interacting with large single-cell RNAseq datasets. loomR provides an interface for working with loom files in a loom-specific way; we provide routines for validating loom files, iterating with chunks through data within the loom file, and provide a platform for other packages to build support for loom files.
|
2024-12-12 |
ucsc-mafsplit
|
public |
Split multiple alignment files
|
2024-12-12 |
snp-dists
|
public |
Convert a FASTA alignment to SNP distance matrix
|
2024-12-12 |
rmath4
|
public |
standalone Rmath library from R
|
2024-12-12 |
mappy
|
public |
Minimap2 Python binding
|
2024-12-12 |
ucsc-pslmap
|
public |
map PSLs alignments to new targets using alignments of
|
2024-12-12 |
pin_hic
|
public |
A Hi-C scaffolding method
|
2024-12-12 |
ucsc-psltobed
|
public |
transform a psl format file to a bed format file.
|
2024-12-12 |
r-soap-nmr
|
public |
No Summary
|
2024-12-12 |
ucsc-crtreeindexbed
|
public |
Create an index for a bed file.
|
2024-12-12 |
mlrho
|
public |
Takes as input a file with assembled reads from a single diploid individual and returns maximum likelihood estimates of the population mutation rate, , the sequencing error , the zygosity correlation, and the population recombination rate.
|
2024-12-12 |
ucsc-bedgeneparts
|
public |
Given a bed, spit out promoter, first exon, or all introns.
|
2024-12-12 |
nemo-age
|
public |
In Nemo-age, it is possible to model genetic and phenotypic evolution in populations with, for instance, overlapping generations, a seed bank, and multiple age classes with stage-specific transition rates, fecundities, selection pressures, and dispersal rates, among other things.
|
2024-12-12 |
seq-gen
|
public |
Seq-Gen is a program that will simulate the evolution of nucleotide or amino acid sequences along a phylogeny, using common models of the substitution process.
|
2024-12-12 |
phyx
|
public |
Phylogenetics tools for linux (and other mostly posix compliant) computers
|
2024-12-12 |
ucsc-pslmappostchain
|
public |
Post genomic pslMap (TransMap) chaining. This takes transcripts that have been mapped via genomic chains adds back in blocks that didn't get include in genomic chains due to complex rearrangements or other issues.
|
2024-12-12 |