CancerVar – Cancer Variants interpretation

CancerVar

:: DESCRIPTION

CancerVar is a bioinformatics software tool for clinical interpretation of somatic variants.

::DEVELOPER

Wang Genomics Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Web Browser

:: DOWNLOAD

CancerVar

:: MORE INFORMATION

Citation

Li Q, Ren Z, Zhou Y, Wang K.
CancerVar: a web server for improved evidence-based clinical interpretation of cancer somatic mutations and copy number abnormalities.
bioRxiv, 2020.

SpeedSeq v0.1.2 – Framework for Rapid Genome Analysis and Interpretation

SpeedSeq v0.1.2

:: DESCRIPTION

SpeedSeq is an open-source genome analysis platform that accomplishes alignment, variant detection and functional annotation of a 50× human genome in 13 h on a low-cost server and alleviates a bioinformatics bottleneck that typically demands weeks of computation with extensive hands-on expert involvement.

::DEVELOPER

The Quinlan Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux
  • Python

:: DOWNLOAD

SpeedSeq

:: MORE INFORMATION

Citation:

Nat Methods. 2015 Oct;12(10):966-8. doi: 10.1038/nmeth.3505. Epub 2015 Aug 10.
SpeedSeq: ultra-fast personal genome analysis and interpretation.
C Chiang, R M Layer, G G Faust, M R Lindberg, D B Rose, E P Garrison, G T Marth, A R Quinlan, and I M Hall.

Knime4Bio – Custom Nodes for the Interpretation of Next Generation Sequencing data with KNIME

Knime4Bio

:: DESCRIPTION

Knime4Bio is a set of custom nodes for the KNIME (The Konstanz Information Miner) graphical workbench, for analysing NGS data without the requirement of programming skills.

::DEVELOPER

Knime4Bio team

:: SCREENSHOTS

:: REQUIREMENTS

  • Linux/ Windows/MacOsX
  • KNIME

:: DOWNLOAD

 Knime4Bio

:: MORE INFORMATION

Citation

Bioinformatics. 2011 Nov 15;27(22):3200-1. doi: 10.1093/bioinformatics/btr554. Epub 2011 Oct 7.
Knime4Bio: a set of custom nodes for the interpretation of next-generation sequencing data with KNIME.
Lindenbaum P, Le Scouarnec S, Portero V, Redon R.

HTSmix 1.0 – Interpretation of High-throughput Perturbation Screens with Low-dimensional Phenotypes

HTSmix 1.0

:: DESCRIPTION

HTSmix represents the structure of signals in the screen using linear mixed models, normalizes and summarizes the phenotypes to make them comparable across samples, and outputs a list of hits while controlling the False Discovery Rate. The methodology is appropriate for experimental designs with at least two control samples profiled throughout the screen.

::DEVELOPER

Laboratory for Statistical Proteomics and Bioinformatics , Purdue University

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux/ MacOsX/ Windows
  • R package

:: DOWNLOAD

 HTSmix

:: MORE INFORMATION

Citation

D. Yu, J. Danku, I. Baxter, S. Kim, O. K. Vatamaniuk, D. E. Salt, O. Vitek.
Noise reduction in genome-wide perturbation screens using linear mixed-effect models”,
Bioinformatics, 27, p. 2173-2180, 2011.

buccaneer 1.5 – Electron Density Interpretation/Protein Model Building software

buccaneer 1.5

:: DESCRIPTION

buccaneer‘ (BUild Connected C-Alphas, Nautical Excuse for Eponym Required) performs statistical chain tracing by identifying connected alpha-carbon positions using a likelihood-based density target.

::DEVELOPER

Kevin Cowtan

:: SCREENSHOTS

N/A

:: REQUIREMENTS

.:: DOWNLOAD

  buccaneer

:: MORE INFORMATION

Citation

Acta Crystallogr D Biol Crystallogr. 2006 Sep;62(Pt 9):1002-11. Epub 2006 Aug 19.
The Buccaneer software for automated model building. 1. Tracing protein chains.
Cowtan K.

Nautilus 0.2 – Electron Density Interpretation/Nucleotide Model Building software

Nautilus 0.2

:: DESCRIPTION

Nautilus‘ (from Greek ναυτίλος, ‘sailor’) is a program for automatic model building of nucleotide structures in electron density maps. It will trace a map with no model, extend an existing model, or add nucleotide chains to an existing non-nucleotide model.

::DEVELOPER

Kevin Cowtan

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux / Mac OsX

:: DOWNLOAD

 Nautilus

:: MORE INFORMATION

LutefiskXP 1.0.7 / Lutefisk – De novo Interpretation of Peptide CID Cpectra

LutefiskXP 1.0.7 / Lutefisk

:: DESCRIPTION

Lutefisk is software for the de novo interpretation of peptide CID spectra.High quality tandem mass spectra of peptides are often obtained for which no exact database match can be made. Consequently, we are faced with the question of whether the protein under investigation is novel, or if the non-matching spectra are due to less exciting prospects such as inter-species variation, database sequence errors, or unexpected proteolytic cleavages. To begin addressing this problem we perform a de novointerpretation of the CID spectra using the computer program Lutefisk; however, any such interpretations nearly always yield multiple sequence candidates, where it is often difficult or impossible to distinguish the correct sequence from the incorrect ones. The variations between candidate sequences are often minor and typically involve dipeptide inversions, swapping of dipeptides of the same mass, replacements of dipeptides with single amino acids of the same mass, and replacements of amino acids by dipeptides of the same mass. We use the multiple sequence candidates produced by Lutefisk as query sequences in a second program, CIDentify. CIDentify is a version of Bill Pearson’s FASTA algorithm modified by Alex Taylor to accommodate MS nuances such as multiple query sequences, ambiguous dipeptides and isobaric mass equivalencies.

::DEVELOPER

Richard S. Johnson( jsrichar@alum.mit.edu)

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux/windows/MacOsX
  • C++ compiler

:: DOWNLOAD

 LutefiskXP

:: MORE INFORMATION

Citation

R. S. Johnson and J. A. Taylor (2002)
Searching sequence databases via de novo peptide sequencing by tandem mass spectrometry“,
Mol. Biotechnology Vol. 22, No. 3. (November 2002), pp. 301-315.

Exit mobile version