10 results in 0.0032 seconds.
-
Benchmark data sets and best practices for WGS/WES somatic mutation detection
The FDA-led MAQC-IV/SEQC2 Consortium has published the data descriptor paper, i.e., Zhao Y. et al. Sci Data (2021), detailing the multi-center multi-platform...Last edited by lethalfang; 11-09-2021, 11:32 AM. -
The Cancer Genome Atlas (TCGA) available in GenePool
GenePool is Station X’s software environment for the management, analysis and sharing of cohort-scale genomics data. GenePool makes it easy for... -
The Duke University breakthrough that could keep your cancer in remission forever
This recent article provides an update on Duke University's development of a microchip device that could make cancer remission permanent:
htt... -
CSHL, UCLA & Einstein to Lead Roundtable Discussions on Single-Cell Sequencing
Open to all attendees, speakers, sponsors, & exhibitors of Single-Cell Sequencing at Next Generation Dx Summit are three roundtable discussions on... -
eSeminar: Genomic Research Panels Overview and Demo
Upcoming eSeminar
Genomic Research Panels Overview and Demo: How to Customize the HaloPlex Cancer Research Panel
Register Today... -
Strelka: Somatic small-variant calling workflow for matched tumor-normal samples
Hello All,
Strelka is a new workflow available to call SNVs and small indels from sequencing data for matched tumor-normal samples. It... -
post-doctoral position in NGS data analysis for cancer study
A post-doctoral research position in next generation sequencing (NGS) data analysis is available at Purdue University. The successful applicant will apply... -
Avadis NGS webinars in July!
New to NGS data analysis?
Sign up for one of our free webinars in July to see how Avadis NGS
can help you analyze RNA-Seq, DNA-S... -
Webinar on Analyzing Cancer Data with Avadis NGS on 30 June!
Join us for a webinar focusing on the analysis of NGS data in the context of cancer biology using the various analysis
and biological interpretation... -
Cancer Genomics using Illumina GA
Hi All
We recently have run cancer samples on Illumina. As this is our first such run, I wanted to know the tools out there to process/analyze...
