• LOC126807510[gene] (9)
  ClinVar
• Exome capture sequencing of 403 barley accessions for the analysis of copy numbe...
  Exome capture sequencing of 403 barley accessions for the analysis of copy number variants

  We exome captured and sequenced 397 diverse barley accessions to carry out a genome-wide analysis copy number variants affecting coding sequences. The Roche Nimblegen exome capture array was used to enrich for exon sequences (http://sequencing.roche.com/products/nimblegen-seqcap-target-enrichment/seqcap-ez-system/seqcap-ez-designs.html). The enriched samples were then sequenced using an Illumina HiSeq 2000 sequencer. An average of 2 x 24.6 million paired end Illumina reads per sample were generated, which correspond to approximately 80x coverage of the 61.3 Mbp exome capture space.
  BioProject
• txid2902495[Organism:exp] (2)
  BioSample

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on