7 results in 0.0030 seconds.
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Failed connection with Ensembl VEP script on port 3337
I'm using the VEP (Variant Effect Predictor) standalone Perl script to annotate some variants, it connects to the Ensembl MySql database. I used the same... -
align reads generated with Nextera exome kit (designed on GRCh37) to GRCh38?
Dear all,
in my lab we are using the Nextera Rapid Capture Exome kit to do whole exome sequencing. Until now I have used GRCh37 as a reference... -
DNA in a chromose
Hi,
I am using the GRCh37 assembly on NCBI website. My question is:
which parts of each chromosome in chr*.fa file is for DNA and... -
Download Human Genome
I want to download assembled human genome from nbci site to calculate some statistics on it. I found GRCh37 in the link below
http://www.ncbi.... -
need GRCh37 database
I am trying to find variants on some bam files I got but GATK requires the exact database used for the alignment.
Apparently it is GRCh37. Any... -
LiftOver coordinate conversion question
Hi,
I'm trying to use UCSC's "LiftOver" tool to convert human genome coordinates from build 36 to build 37. Some positions and... -
RepeatMasker report of GRCh37
Hi everyone,
I recently used RepeatMasker to analyze the DNA sequences of broken fragments of some cancer patients' chromosomes. I finnaly...
