Hello everybody,
It is my first time working with cancer genomes and I have some doubts. I found this study in which they provide a lot of...
9 results in 0.0021 seconds.
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Using Copy Number Alterations detected in other studies for the same tumor cell line
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Bioinformatic Analysis of Next Generation Sequencing Data @NIH,USA February 6-9, 2018
Training in Bioinformatic Analysis of Next Generation Sequencing Data
February 6-9, 2018
Where?
National Institutes... -
Sample data
Where can I get whole genome sequencing data of case and control for a particular disease.
I need specifically the normal and the diseased specifically... -
Hello everyone!!
I'm a new research from Brazil who works with T. cacao, if someone likes chocolate so we have something in common. I'm writing a project to develop RAD-Seq... -
How to get the files of pair end read!
I'm new in the region.
I wanna learn how to use the softwares such as BWA, Pindel, etc.
But I don't have the data of the sequence and the... -
raw sequence short read data
Hi,
Does anyone know where I can find raw short read sequence data? By raw, I mean unfiltered, so that the low quality reads from the... -
short read qualities for various NGS machines
Hi,
I am looking for the DNA sequence coverage profiles for the human genome for various different sequencing machines, such as Illumina... -
small part of all 1000 sequences from 1000genomes data needed?
Hi,
I am a newbie to next-gen data (just working from past couple of days). I am working on 1000genomes data for my thesis work.
... -
ICBR at University of Florida adopts GenomeQuest SDM Platform
Hey Everyone,
The Interdisciplinary Center for Biotechnology Research (ICBR) at the University of Florida is adopting the GenomeQuest platform...
