Currently it supports processing data from HiSeq 2000/2500/3000/4000, Nextseq 500/550, MiniSeq.and other Illumina 1.8 or newer formats.Īnother Gff Analysis Toolkit (AGAT). AfterQC can simply go through all fastq files in a folder and then output three folders: good, bad and QC folders, which contains good reads, bad reads and the QC results of each fastq file/pair. 2012) is a software package that supports formal tests of whether admixture occurred, and makes it possible to infer admixture proportions and dates.ĪFNI is a suite of programs for looking at and analyzing 3D brain images.Īutomatic Filtering, Trimming, Error Removing and Quality Control for fastq data. Mass screening of contigs for antibiotic resistance genesĪutoDockFR (or ADFR in short) is a protein-ligand docking program developed in the Sanner laboratory at Scripps Research under the AutoDock umbrellaĪDMIXTOOLS (Patterson et al. StringTie is a fast and highly efficient assembler of RNA-Seq alignments into potential transcripts.ĪBACAS is intended to rapidly contiguate (align, order, orientate), visualize and design primers to close gaps on shotgun assembled contigs based on a reference sequence.Ībaqus is a software suite for finite element analysis and computer-aided engineering.ĪBayesQR is a viral quasispecies reconstruction algorithm that employs a maximum-likelihood framework to infer individual sequences in a mixture from high-throughput sequencing data.ĪBINIT is an atomic-scale simulation software suite. RAPSearch2 is a tool for fast protein similarity searches. R is a free software environment for statistical computing and graphics. The MEME suite is a collection of tools for the discovery and analysis of sequence motifs. 3D Slicer is a free, open source and multi-platform software package widely used for medical, biomedical, and related imaging research.īIC-seq can accurately and efficiently identify CNVs via minimizing the Bayesian information criterion.ĬNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing.Ĭompiler/intel/20 compiler/gcc/11 compiler/pgi/20 compiler/intel/19 compiler/gcc/10
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