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tinycov: standalone command line utility written in python to plot coverage from a BAM file
By Jit 2326 days agogithub.com - Tinycov is a small standalone command line utility written in python to plot the coverage of a BAM file quickly. This software was inspired by Matt Edwards' genome coverage plotter. To install the stable version: pip3 install --user...GraphMap - A highly sensitive and accurate mapper for long, error-prone reads
By Jit 3346 days agogithub.com - GraphMap - A highly sensitive and accurate mapper for long, error-prone reads http://www.nature.com/ncomms/2016/160415/ncomms11307/full/ncomms11307.htmlFeatures Mapping position agnostic to alignment parameters. ...HISAT2: a fast and sensitive alignment program for mapping next-generation sequencing reads
By Rahul Nayak 3011 days agogithub.com - HISAT2 is a fast and sensitive alignment program for mapping next-generation sequencing reads (both DNA and RNA) to a population of human genomes (as well as to a single reference genome). Based on an extension of BWT for...GenomeMapper: Simultaneous alignment of short reads against multiple genomes
By Jit 2994 days ago1001genomes.org - GenomeMapper is a short read mapping tool designed for accurate read alignments. It quickly aligns millions of reads either with ungapped or gapped alignments. It can be used to align against multiple genomes simulanteously or against a single...ReMILO: reference assisted misassembly detection algorithm using short and long reads.
By Jit 2952 days agogithub.com - ReMILO, a reference assisted misassembly detection algorithm that uses both short reads and PacBio SMRT long reads. ReMILO aligns the initial short reads to both the contigs and reference genome, and then constructs a novel data structure called...PANDASEQ is a program to align Illumina reads, optionally with PCR primers embedded in the...
By BioStar 2875 days agogithub.com - Development packages for zlib and libbz2 are needed, as well as a standard compiler environment. On Ubuntu, this can be installed via: sudo apt-get install build-essential libtool automake zlib1g-dev libbz2-dev pkg-config On MacOS, the Apple...Flye: Fast and accurate de novo assembler for single molecule sequencing reads
By Rahul Nayak 2587 days agogithub.com - Flye is a de novo assembler for single molecule sequencing reads, such as those produced by PacBio and Oxford Nanopore Technologies. It is designed for a wide range of datasets, from small bacterial projects to large mammalian-scale assemblies. The...Filtlong: quality filtering tool for long reads
By Radha Agarkar 2275 days agogithub.com - Filtlong is a tool for filtering long reads by quality. It can take a set of long reads and produce a smaller, better subset. It uses both read length (longer is better) and read identity (higher is better) when choosing which reads pass the...FastProNGS: fast preprocessing of next-generation sequencing reads
By Rahul Nayak 2048 days agogithub.com - FastProNGS to integrate the quality control process with automatic adapter removal. Parallel processing was implemented to speed up the process by allocating multiple threads. Compared with similar up-to-date preprocessing tools, FastProNGS is by...Steps to find palindrome in genomes !
By BioStar 1245 days agoPalindromes are sequences of nucleotides that read the same backward as forward.
