pevsnerlab.kennedykrieger.org - DRAGON: Database Referencing of Array Genes Online
SNOMAD: Standardization and Normalization of Microarray Data
SNPduo: SNP Analysis Between Two Individuals
SNPtrio: Analyzing and Visualizing and Inheritance Patterns in Trios
SNPscan: Data...
www.genome.gov - What is the epigenome?
What does the epigenome do?
What makes up the epigenome?
Is the epigenome inherited?
What is imprinting?
Can the epigenome change?
What makes the epigenome change?
How do changes in the epigenome contribute to...
CSIR - Institute of Himalayan Bioresource Technology 2 vacancies of Project Fellow
Name of the Post: Project Fellow
No. of the Post: 02 Two
Salary: Rs. 12000/- per month or Rs. 14000/- per month
Age Limit: Max. 28 years as on 10.06.2015...
kallisto
Transcript abundance quantification from RNA-seq data (uses pseudoalignment for rapid determination of read compatibility with targets)
Software (C++)
https://pachterlab.github.io/kallisto/
Sailfish
Estimation of isoform abundances...
sourceforge.net - AIRVF that works on flowgram, raw and mapped reads and called variants to reduce artifact-driven false variant calls. Tests on sequencing data of standard reference material showed up to ∼98% reduction of false variants when combined to...
The IPython Notebook is a web-based interactive computational environment where you can combine code execution, text, mathematics, plots and rich media into a single document
github.com - Heap, that enables robustly sensitive and accurate calling of SNPs, particularly with a low coverage NGS data, which must be aligned to the reference genome sequences in advance. To reduce false positive SNPs, Heap determines genotypes and calls...