Oct 30 2019
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phantompeakqualtools
Phantompeakqualtools computes informative enrichment and quality measures for ChIP-seq/DNase-seq/FAIRE-seq/MNase-seq data. It can also be used to obtain robust estimates of the predominant fragment length or characteristic tag shift values in these assays.
Updated versions:
1.2.1.1 | Linux 64
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Oct 24 2019
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deepTools
a suite of python tools particularly developed for the efficient analysis of high-throughput sequencing data, such as ChIP-seq, RNA-seq or MNase-seq.
Updated versions:
3.3.1 | OS X INTEL
3.3.1 | Linux 64
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Oct 21 2019
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HTSeq
a Python package that provides infrastructure to process data from high-throughput sequencing assays.
Updated versions:
0.9.1 | Linux 64
0.6.1 | Linux 64
0.9.1 | OS X INTEL
0.11.2 | OS X INTEL
0.11.2 | Linux 64
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Oct 17 2019
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MACS2
(Model Based Analysis of ChIP-Seq data) a novel algorithm for identifying transcript factor binding sites.
Updated versions:
2.2.4 | Linux 64
2.2.4 | OS X INTEL
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Oct 16 2019
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FASTA
a DNA and protein sequence alignment software package that searches for matching sequence patterns or words, called k-tuples.
Updated versions:
14-aug-2019 | Linux 64
14-aug-2019 | OS X INTEL
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Oct 16 2019
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PyMC3
PyMC3 is a Python package for Bayesian statistical modeling and Probabilistic Machine Learning focusing on advanced Markov chain Monte Carlo (MCMC) and variational inference (VI) algorithms. Its flexibility and extensibility make it applicable to a large suite of problems.
Updated versions:
3.7 | Linux 64
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Oct 16 2019
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MapCaller
An efficient and versatile approach for short-read alignment and variant detection in high-throughput sequenced genomes.
Updated versions:
0.9.9.17 | OS X INTEL
0.9.9.17 | Linux 64
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Oct 15 2019
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SPAdes
(St. Petersburg genome assembler) a genome assembly algorithm designed for single-cell and multi-cell bacterial data sets.
Updated versions:
3.13.1 | Linux 64
3.13.1 | OS X INTEL
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Oct 15 2019
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RStudio
an integrated development environment (IDE) for R that includes a console, syntax-highlighting editor that supports direct code execution, as well as tools for plotting, history, debugging and workspace management.
Updated versions:
1.2.5001 | OS X INTEL
1.2.5001 | Linux 64
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Oct 10 2019
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Slingshot
an R package that provides functions for inferring continuous, branching lineage structures in low-dimensional data. Designed to model developmental trajectories in single-cell RNA sequencing data and serve as a component in an analysis pipeline after dimensionality reduction and clustering, Slingshot is flexible enough to handle arbitrarily many branching events and allows for the incorporation of prior knowledge through supervised graph construction.
Updated versions:
1.3.2 | OS X INTEL
1.3.2 | Linux 64
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Oct 03 2019
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Oncofuse
Oncofuse is a framework designed to estimate the oncogenic potential of de-novo discovered gene fusions. It uses several hallmark features and employs a bayesian classifier to provide the probability of a given gene fusion being a driver mutation.
Updated versions:
1.1.1 | OS X INTEL
1.1.1 | Linux 64
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Oct 03 2019
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GROOT
GROOT is a tool to type Antibiotic Resistance Genes (ARGs) in metagenomic samples (a.k.a. Resistome Profiling). It combines variation graph representation of gene sets with an LSH indexing scheme to allow for fast classification of metagenomic reads. Subsequent hierarchical local alignment of classified reads against graph traversals facilitates accurate reconstruction of full-length gene sequences using a simple scoring scheme.
Updated versions:
0.8.5 | OS X INTEL
0.8.5 | Linux 64
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Oct 03 2019
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Parafly
Given a file containing a list of unix commands, multithreading is used to process the commands in parallel on a single server. Success/failure is captured, and failed commands are retained and reported.
Updated versions:
r2013_01_21 | Linux 64
r2013_01_21 | OS X INTEL
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Oct 02 2019
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anvi'o
an open-source, community-driven analysis and visualization platform for ‘omics data. Its interactive interface facilitates the management of metagenomic contigs and associated data for automatic or human-guided identification of genome bins and their curation.
Updated versions:
5.5.0 | Linux 64
5.5.0 | OS X INTEL
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Oct 02 2019
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slclust
slclust is a utility that performs single-linkage clustering with the option of applying a Jaccard similarity coefficient to break weakly bound clusters into distinct clusters.
Updated versions:
02022010 | OS X INTEL
02022010 | Linux 64
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Oct 02 2019
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Fastool
Fastool is a simple and quick tool to read huge FastQ and FastA files (both normal and gzipped) and manipulate them.
It makes use of the KSeq library (http://lh3lh3.users.sourceforge.net/kseq.shtml) for fast access to FastQ/A files.
Updated versions:
0.1.4 | OS X INTEL
0.1.4 | Linux 64
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Oct 02 2019
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Circlator
Circlator is a tool to circularize genome assemblies. The input is a genome assembly in FASTA format and corrected PacBio or nanopore reads in FASTA or FASTQ format. Circlator will attempt to identify each circular sequence and output a linearised version of it. It does this by assembling all reads that map to contig ends and comparing the resulting contigs with the input assembly.
Updated versions:
1.5.5 | OS X INTEL
1.5.5 | Linux 64
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Oct 02 2019
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Pilon
Pilon is a software tool which can be used to automatically improve draft assemblies and find variation among strains, including large event detection.
Updated versions:
1.23 | OS X INTEL
1.23 | Linux 64
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Oct 02 2019
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Canu
Canu is a fork of the Celera Assembler designed for high-noise single-molecule sequencing. Canu specializes in assembling PacBio or Oxford Nanopore sequences. Canu operates in three phases: correction, trimming and assembly. The correction phase will improve the accuracy of bases in reads.
Updated versions:
1.5 | OS X INTEL
1.8 | Linux 64
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Oct 01 2019
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bam2fastx
bam2fastx provides conversion of PacBio BAM files into gzipped fasta and fastq files, including splitting of barcoded data.
Updated versions:
1.3.0 | Linux 64
1.3.0 | OS X INTEL
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