MetaCherchant – Analysing Genomic Environment of a Nucleotide Sequence within a Metagenome

MetaCherchant

:: DESCRIPTION

MetaCherchant is a tool for analyzing genomic context of antibiotic resistance genes in gut microbiota.

::DEVELOPER

Computer Technologies Laboratory, National Research University of Information Technologies,

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux / Windows / MacOs
  • JRE
:: DOWNLOAD

MetaCherchant

:: MORE INFORMATION

Citation

Olekhnovich EI, Vasilyev AT, Ulyantsev VI, Kostryukova ES, Tyakht AV.
MetaCherchant: analyzing genomic context of antibiotic resistance genes in gut microbiota.
Bioinformatics. 2018 Feb 1;34(3):434-444. doi: 10.1093/bioinformatics/btx681. PMID: 29092015.

AncestralClust – Cluster Divergent Sequences

AncestralClust

:: DESCRIPTION

AncestralClust is a clustering program, which is developed for clustering divergent sequences.

::DEVELOPER

Lenore Pipes @ Nielsen Berkeley Lab

:: SCREENSHOTS

N/A

::REQUIREMENTS

  • Linux

:: DOWNLOAD

AncestralClust

:: MORE INFORMATION

Citation

Pipes L, Nielsen R.
AncestralClust: Clustering of Divergent Nucleotide Sequences by Ancestral Sequence Reconstruction using Phylogenetic Trees.
Bioinformatics. 2021 Oct 20:btab723. doi: 10.1093/bioinformatics/btab723. Epub ahead of print. PMID: 34668516.

ProSeqViewer 1.0.42 – Visualize Sequence and Multiple Sequence Alignment (MSA)

ProSeqViewer 1.0.42

:: DESCRIPTION

ProSeqViewer is a TypeScript library to visualize annotation on single sequences and multiple sequence alignments.

::DEVELOPER

The BioComputing UP lab

:: SCREENSHOTS

:: REQUIREMENTS

  • Linux / Windows
  • JS

:: DOWNLOAD

ProSeqViewer

:: MORE INFORMATION

Citation:

Bevilacqua M, Paladin L, Tosatto SCE, Piovesan D.
ProSeqViewer: an interactive, responsive and efficient TypeScript library for visualization of sequences and alignments in web applications.
Bioinformatics. 2021 Nov 12:btab764. doi: 10.1093/bioinformatics/btab764. Epub ahead of print. PMID: 34788797.

DiagAF 21.2.7 – Pre-Alignment Filter for Sequence Alignment

DiagAF 21.2.7

:: DESCRIPTION

DiagAF is a more accurate and efficient pre-alignment filter for sequence alignment. It can efficiently filter out candidates that contain errors greater than the edit distance threshold during read mapping.

::DEVELOPER

DiagAF team

:: SCREENSHOTS

N/a

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

DiagAF

:: MORE INFORMATION

Citation

Yu C, Zhao Y, Zhao C, Ma H, Wang G.
DiagAF: A More Accurate and Efficient Pre-Alignment Filter for Sequence Alignment.
IEEE/ACM Trans Comput Biol Bioinform. 2021 Nov 17;PP. doi: 10.1109/TCBB.2021.3127879. Epub ahead of print. PMID: 34780330.

RNA-unchained v1.0 – Chaining sequence/structure seeds for computing RNA Similarity

RNA-unchained v1.0

:: DESCRIPTION

RNA-unchained aims at detecting structural homologs of a given query RNA sequence in a, potentially large, collection of RNA structures.

::DEVELOPER

Computational Methods for Paleogenomics and Comparative Genomics

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux
  • Python

:: DOWNLOAD

RNA-unchained

:: MORE INFORMATION

Citation

Bourgeade L, Chauve C, Allali J.
Chaining sequence/structure seeds for computing RNA similarity.
J Comput Biol. 2015 Mar;22(3):205-17. doi: 10.1089/cmb.2014.0283. PMID: 25768236.

MUMmerGPU 2.0 – High-throughput sequence alignment using GPU

MUMmerGPU 2.0

:: DESCRIPTION

MUMmerGPU is an open-source high-throughput parallel pairwise local sequence alignment program that runs on commodity Graphics Processing Units (GPUs) in common workstations. MUMmerGPU uses the new Compute Unified Device Architecture (CUDA) from nVidia to align multiple query sequences against a single reference sequence stored as a suffix tree. By processing the queries in parallel on the highly parallel graphics card, MUMmerGPU achieves more than a 10-fold speedup over a serial CPU version of the sequence alignment kernel, and outperforms the exact alignment component of MUMmer on a high end CPU by 3.5-fold in total application time when aligning reads from recent sequencing projects using Solexa/Illumina, 454, and Sanger sequencing technologies. MUMmerGPU is a low cost, ultra-fast sequence alignment program designed to handle the increasing volume of data produced by new, high-throughput sequencing technologies.

::DEVELOPER

Michael Schatz

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux
  • nVidia Card

:: DOWNLOAD

MUMmerGPU

:: MORE INFORMATION

MUMmerGPU is an open source project.

Citation:

Cole Trapnell and Michael C. Schatz
Optimizing data intensive GPGPU computations for DNA sequence alignment
Parallel Computing 2009 35(8-9)429-440

SIBIS 1.0 – Bayesian model for Inconsistent Protein Sequence Estimation

SIBIS 1.0

:: DESCRIPTION

SIBIS (Bayesian Inconsistency in Sequences) is designed to detect such inconsistencies based on the evolutionary information in multiple sequence alignments. A Bayesian framework, combined with Dirichlet mixture models, is used to estimate the probability of observing specific amino acids and to detect inconsistent or erroneous sequence segments.

::DEVELOPER

Julie Dawn Thompson

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 SIBIS

:: MORE INFORMATION

Citation

Bioinformatics. 2014 May 13. pii: btu329. [Epub ahead of print]
SIBIS: A Bayesian model for inconsistent protein sequence estimation.
Khenoussi W1, Vanhoutrève R1, Poch O1, Thompson JD2.

FSTVAL – Flanking Sequence Tag Validator

FSTVAL

:: DESCRIPTION

FSTVAL is an open access web tool to manage bulk flanking sequence tags (FSTs).FSTVAL automatically evaluates the FSTs and finds the best mapping positions of the FST against a known genome sequence.

::DEVELOPER

FSTVAL team

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux

:: DOWNLOAD

 FSTVAL

:: MORE INFORMATION

Citation

Plant Methods. 2012 Jun 18;8(1):19. doi: 10.1186/1746-4811-8-19.
FSTVAL: a new web tool to validate bulk flanking sequence tags.
Kim JS1, Kim J, Lee TH, Jun KM, Kim TH, Kim YH, Park HM, Jeon JS, An G, Yoon UH, Nahm BH, Kim YK.

rvsel 0.1 – Rare Variants Selection with Sequence Data

rvsel 0.1

:: DESCRIPTION

rvsel is an R package for rare variants selection with sequence data. The most outome-related rare variants are selected within a gene or a genetic region. The selection procedure is based on the power set of the subset of the rare variants.

::DEVELOPER

Wang Lab @ Biostatistics Department

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux
  • R

:: DOWNLOAD

 rvsel

:: MORE INFORMATION

Citation

Bioinformatics. 2014 Apr 22. pii: btu207.
A power set-based statistical selection procedure to locate susceptible rare variants associated with complex traits with sequencing data.
Sun H, Wang S.

bam2fastq 1.1.0 – Extract Sequences from a BAM file in Fastq format

bam2fastq 1.1.0

:: DESCRIPTION

bam2fastq is a program to extract sequences and qualities from a BAM file.

::DEVELOPER

The Genomic Services Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux
  • C++ Compiler
:: DOWNLOAD

 bam2fastq

:: MORE INFORMATION

Exit mobile version