biodockerfiles

• admixture-1.3.0: ADMIXTURE is a software tool for maximum likelihood estimation of individual ...
• annotsv-3.2.1: AnnotSV is a standalone program designed for annotating and ranking Structura...
• atropos-1.1.22: Atropos is tool for specific, sensitive, and speedy trimming of NGS reads and...
• autodock-vina-1.2.3: AutoDock Vina is a turnkey computational docking program that is based on a s...
• bbmap-38.79: BBTools is a suite of fast, multithreaded bioinformatics tools designed for a...
• bcftools-1.10.2: BCFtools is a set of utilities that manipulate variant calls in the Variant C...
• bcftools-1.13: BCFtools is a set of utilities that manipulate variant calls in the Variant C...
• bcftools-1.9: BCFtools is a set of utilities that manipulate variant calls in the Variant C...
• beagle-5.1-24Mar20.5f5: Beagle is a software package for phasing genotypes and for imputing ungenotyp...
• bedops-2.4.39: BEDOPS is an open-source command-line toolkit that performs highly efficient ...
• fastq-screen-0.14.0: FastQ Screen allows you to screen a library of sequences in FastQ format agai...
• fastq-screen-0.15.2: FastQ Screen allows you to screen a library of sequences in FastQ format agai...
• fastqc-0.11.9: FastQC aims to provide a simple way to do some quality control checks on raw ...
• jasmine-1.1.4: This tool is used to merge structural variants (SVs) across samples.
• manta-1.5.0: Manta calls structural variants (SVs) and indels from mapped paired-end seque...
• plink-1.07: PLINK is a free, open-source whole genome association analysis toolset, desig...
• plink-1.90b6.16: PLINK is a free, open-source whole genome association analysis toolset, desig...
• rdkit-2016.03.5: RDKit is a collection of cheminformatics and machine-learning software writte...
• rtg-tools-3.10.1: RTG Tools contains utilities to easily manipulate and accurately compare mult...
• sambamba-0.7.1: Sambamba is a high performance highly parallel robust and fast tool (and libr...
• samtools-1.10: Samtools is a suite of programs for interacting with high-throughput sequenci...
• samtools-1.20: Samtools is a suite of programs for interacting with high-throughput sequenci...
• seqtk-1.2: Seqtk is a fast and lightweight tool for processing sequences in the FASTA or...
• staden-2.0.0b11-2016: A fully developed set of DNA sequence assembly (Gap4 and Gap5), editing and a...
• survivor-1.0.7: SURVIVOR is a tool set for simulating/evaluating SVs, merging and comparing S...
• svviz2-2.0a3: svviz2 is used to evaluate and visualize candidate structural variants. svviz...
• treemix-1.12: TreeMix is a method for inferring the patterns of population splits and mixtu...
• trim-galore-0.4.4: Trim Galore! is a wrapper script to automate quality and adapter trimming as ...
• verifybamid-1.1.3: verifyBamID is a software that verifies whether the reads in particular file ...
• vt-0.57721: vt is a variant tool set that discovers short variants from Next Generation S...

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