malder
|
public |
MALDER is a version of ALDER (http://groups.csail.mit.edu/cb/alder/) that has been modified to allow multiple admixture events.
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2024-12-12 |
ucsc-bigwigcat
|
public |
merge non-overlapping bigWig files
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2024-12-12 |
ucsc-pslselect
|
public |
select records from a PSL file.
|
2024-12-12 |
ucsc-bigwigmerge
|
public |
Merge together multiple bigWigs into a single output bedGraph.
|
2024-12-12 |
ucsc-pslmrnacover
|
public |
Make histogram of coverage percentage of mRNA in psl.
|
2024-12-12 |
poplddecay
|
public |
PopLDdecay: a fast and effective tool for linkage disequilibrium decay analysis based on variant call format (VCF) files.
|
2024-12-12 |
fusioncatcher-seqtk
|
public |
This is modified Seqtk version required for FusionCatcher.
|
2024-12-12 |
gsalign
|
public |
GSAlign: an ultra-fast sequence alignment tool
|
2024-12-12 |
f5c
|
public |
An optimised re-implementation of the call-methylation and eventalign modules in Nanopolish.
|
2024-12-12 |
hr2
|
public |
HR2 is a program to calculate elemental compositions for a given mass. This program and its documentation are Copyright (c) 1992-2005 by Joerg Hau
|
2024-12-12 |
segul
|
public |
An ultrafast and memory efficient tool for phylogenomics
|
2024-12-12 |
ucsc-mafspeciessubset
|
public |
Extract a maf that just has a subset of species.
|
2024-12-12 |
fastq-and-furious
|
public |
Fast handling of FASTQ files
|
2024-12-12 |
ucsc-hgloadnet
|
public |
Load a generic net file into database
|
2024-12-12 |
amplisim
|
public |
Plain simple amplicon sequence simulator for in-silico genomic sequencing assays.
|
2024-12-12 |
bed2gtf
|
public |
A high-performance BED-to-GTF converter written in Rust
|
2024-12-12 |
tantan
|
public |
tantan masks simple regions (low complexity & short-period tandem repeats) in biological sequences.
|
2024-12-12 |
fgwas
|
public |
fgwas is a command line tool for integrating functional genomic information into a genome-wide association study (GWAS).
|
2024-12-12 |
ucsc-hgloadout
|
public |
load RepeatMasker .out files into database
|
2024-12-12 |
r-biodb
|
public |
An R package for connecting to chemical and biological databases.
|
2024-12-12 |
consensify
|
public |
A method for generating a consensus pseudohaploid genome sequence
|
2024-12-12 |
fastk
|
public |
FastK is a k‑mer counter that is optimized for processing high quality DNA assembly data sets such as those produced with an Illumina instrument or a PacBio run in HiFi mode.
|
2024-12-12 |
gffcompare
|
public |
GffCompare by Geo Pertea
|
2024-12-12 |
raxml-ng
|
public |
RAxML Next Generation: faster, easier-to-use and more flexible
|
2024-12-12 |
boutroslabplottinggeneral
|
public |
No Summary
|
2024-12-12 |
ucsc-fastqtofa
|
public |
Convert from fastq to fasta format.
|
2024-12-12 |
ucsc-hgloadmaf
|
public |
Load a maf file index into the database
|
2024-12-12 |
prot-scriber
|
public |
Assigns short human readable descriptions (HRD) to query biological sequences using reference candidate descriptions.
|
2024-12-12 |
conifer
|
public |
Calculate confidence scores from Kraken2 output
|
2024-12-12 |
bustools
|
public |
bustools is a program for manipulating BUS files for single cell RNA-Seq datasets.
|
2024-12-12 |
miniprot-boundary-scorer
|
public |
Miniprot boundary scorer parses introns, starts, stops and exons from miniprot's alignment output and scores them
|
2024-12-12 |
tidk
|
public |
Identify and find telomeres, or telomeric repeats in a genome.
|
2024-12-12 |
ucsc-mafaddqrows
|
public |
Add quality data to a maf
|
2024-12-12 |
core-snp-filter
|
public |
Filtering sites (i.e. columns) in a FASTA-format whole-genome pseudo-alignment.
|
2024-12-12 |
ucsc-mafsinregion
|
public |
Extract MAFS in a genomic region
|
2024-12-12 |
ucsc-farc
|
public |
Reverse complement a FA file
|
2024-12-12 |
ucsc-maftosnpbed
|
public |
finds SNPs in MAF and builds a bed with their functional consequence
|
2024-12-12 |
ucsc-maskoutfa
|
public |
Produce a masked .fa file given an unmasked .fa and
|
2024-12-12 |
ucsc-gff3topsl
|
public |
convert a GFF3 CIGAR file to a PSL file
|
2024-12-12 |
smudgeplot_rn
|
public |
Inference of ploidy and heterozygosity structure using whole genome sequencing data. Fork of Kamil S. Jarons Smudgeplot.
|
2024-12-12 |
pgenlib
|
public |
Python wrapper for pgenlib's basic reader and writer.
|
2024-12-12 |
bayestyper
|
public |
A method for variant graph genotyping based on exact alignment of k-mers
|
2024-12-12 |
est-sfs
|
public |
est-sfs ( Keightley and Jackson, 2018) is a stand-alone implementation of a method to infer the unfolded site frequency spectrum (the uSFS) and ancestral state probabilities by maximum likelihood (ML).
|
2024-12-12 |
links
|
public |
Long Interval Nucleotide K-mer Scaffolder
|
2024-12-12 |
r-momf
|
public |
The package can fit single RNA-seq data set(SOMF) and multiple RNA-seq data sets (MOMF).
|
2024-12-12 |
derna
|
public |
RNA sequence design for a target protein sequence.
|
2024-12-12 |
gum
|
public |
A header-only library for representation of sequence graphs
|
2024-12-12 |
mbg
|
public |
Minimizer based sparse de Bruijn graph constructor
|
2024-12-12 |
daligner
|
public |
DALIGNER: Find all significant local alignments between reads
|
2024-12-12 |
riblast
|
public |
RIblast is ultrafast RNA-RNA interaction prediction software.
|
2024-12-12 |