Data

Genomics Virtual Laboratory (GVL) Tutorials: Detecting small variants (SNVs and indels) using Galaxy workflow Input

QFAB
Andrew Lonie (Associated with)
Viewed: [[ro.stat.viewed]] Cited: [[ro.stat.cited]] Accessed: [[ro.stat.accessed]]
ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=http://galaxy-tut.genome.edu.au/u/alonie/h/variantdetectionbasicprep&rft.title=Genomics Virtual Laboratory (GVL) Tutorials: Detecting small variants (SNVs and indels) using Galaxy workflow Input&rft.identifier=www.qfab.org/GVL/input-collection-5&rft.publisher=QFAB&rft.description=Short read data from the exome of chromosome 22 of a single human individual. There are one million 76bp reads in the dataset, produced on an Illumina GAIIx from exome-enriched DNA. This data was generated as part of the 1000 Genomes project: http://www.1000genomes.org/. Please use the ‘fastqsanger’ File Format&rft.creator=Anonymous&rft.date=2013&rft.type=dataset&rft.language=English Access the data
Cite Saved to MyRDA Save to MyRDA

Access:

Other view details

CC-BY http://creativecommons.org.au/learn-more/licences


Full description

Short read data from the exome of chromosome 22 of a single human individual. There are one million 76bp reads in the dataset, produced on an Illumina GAIIx from exome-enriched DNA. This data was generated as part of the 1000 Genomes project: http://www.1000genomes.org/. Please use the ‘fastqsanger’ File Format

This dataset is part of a larger collection

Click to explore relationships graph
Help

Related People

Related Services

User Contributed Tags    

Login to tag this record with meaningful keywords to make it easier to discover

Identifiers
  • Local : www.qfab.org/GVL/input-collection-5
Similar data you may be interested in:
See more Integrated Biological Discovery data