Results for "structural and sequence variation"
News
Update Genome Workbench 2.7.15 released
NCBI Genome Workbench is an integrated application for viewing and analyzing sequence data. With Genome Workbe...data in publically available sequence databases at NCBI, and mix this data with your own p...ion for viewing and analyzing sequence data. Genome Workbench was de...3722 days ago
- A team from Cold Spring Harbor Laboratory has released an algor...Scalpel, which is open source and available for download on Sou...n test runs on both simulated and real whole human exomes. Lik...genome, to account for simple sequence repeats that are a regular so...es), splits them into k-mers, and creat...
3547 days ago
The 8000 years old Tibetian gene mutation !!!
A new study has provided insight into how gene mutation around 8,0...ange that dates back 8,000 years and demonstrate how it contribute...ent of Tibetans have the genetic variation, and it was virtually absent from closel...he findings indicate the genetic variation endows its carriers with an a...3546 days ago
Surrogate Variable Analysis (SVA)
The sva package contains functions for removing batch effects and other unwanted variation in high-throughput expe...three ways: (1) identifying and esti...iables for unknown sources of variation in high-throughput experiment...Xiv). Removing batch effects and using surrogate variables in differ...3476 days ago
Roche has acquired Bina Technologies !!!
Bina Technologies is a privately held company that provides a b...rm for centralized management and processing of next generation...g (NGS) data for the academic and translational research market...r secondary genomic analysis, sequence alignment, and variant calling, but since 2012, i...3415 days ago
- What is new? Expansion of Protists and Fungi with hundreds of annotated genomes Variation data for bread wheat, rice, Aedes aegypti, and Ixodes scapularis Whole genome alignments for O. longistaminata and T. cacao Non-coding RNA gene model...
3247 days ago
- ...emical reaction to encode the sequence of a DNA molecule into a...surable surrogate called an Xpandomer. This single molecule approach produces enough Xpandomer in a single drop reaction to sequence an entire human genome 1000X...expansion technology. The DNA sequence is then read out as the Xpandomer r...
3246 days ago
Webinar on Streamlining large scale analysis using the Strand NGS Pipeline Manager on 24 Feb 2016
Live Webinar on Streamlining large scale NGS data analysis using the Strand NGS Pipeline Manager on 24 Feb 2016 Abstract: Strand NGS includes comprehensive wo...NGS allows users to execute a sequence of analysis steps with s...kaged pipelines present in Strand NGS. The packaged pipelines have w...3013 days ago
- MutaBind is a new computational method and server created through NCBI researc...ts that maps mutations on a protein structural complex, calculates ch...y, identifies deleterious mutations and produces a downloadable mutant structur...ng with selecting a protein complex and input...
2891 days ago
- Genome Workbench 2.10.7 is here! New features include added sup...om BLAST databases Graphical Sequence View: added log scaling...orial added Bug Fixes and Improvements Project Tree View:...ank could resolve to the same sequence Graphical Sequence View: fix...
2866 days ago
