Computer simulation of genetic mechanism !!
...gle.com/p/treesimj/ Variant Simulation Tools A simulation tool for post-GWAS genetic epidemiological studies using whole-genome or whole-exome next-gen sequencing data, wit...2989 days ago
Tools and Method for Haplotype phasing !
...advances, both from increasingly comprehensive and inexpensive genome-wide SNP microarrays and from ever more accessible whole-genome and whole-exome sequencing methods. The vast...1353 days ago
Next Generation Sequencing (NGS) Tutorials
...; DOI: 10.1186/1471-2105-12-134 Abstract: http://www.biomedcentral.com/1471-2105/12/134/abstract WEP: a high-performance analysis pipeline for whole-exome data http://www.biomedce...3502 days ago
3667 days ago
List of Bioinformatics Software Tools for Next Generation Sequencing
...ml or plain text format, graphical display of results Exomiser Description: Wellcome Trust Sanger; functionally annotates variants from whole-exome sequencing data; Based on Jan...2923 days ago
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Clinical Genomics & Informatics Europe at Lisbon, Portugal
Bio-IT World and Cambridge Healthtech Institute's fifth international Clinical Genomics & Informatics Europe conference will feature four main tracks on Clinical Exom...3931 days ago
Assistant Professor @ King Saud University Riyadh
Qualifications: Candidates must have a Ph.D. and a strong background in Molecular and Cellular Biology, protein expression, FACS, or computational biology, and ability to...3740 days ago
1952 days ago
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
EXCAVATOR, for the detection of copy number variants (CNVs) from whole-exome sequencing data. EXCAVATOR combines a three-step normalization procedure with a novel heterogeneous hidden Markov model algorithm and a calling method that classifies genomic regions into five copy number states. We vali...Tags: EXCAVATOR, detect, copy, number, variants, whole-exome, sequencing, data
1962 days ago
Comment on "List of popular bioinformatics software/tools"
There are different ways to perform exome sequence analysis, but GATK have a good guide for 'Best Practice': http://www.broadinstitute.org/gatk/guide/best-practices3602 days ago