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SRX000113: 454 sequencing of Human James D. Watson genomic fragment library
8 LS454 (454 GS FLX) runs: 1.2M spots, 316.3M bases, 754.8Mb downloads

Design: None provided.
Submitted by: Cold Spring Harbor Laboratory
Study: Genome sequence of Dr. James D. Watson.
show Abstracthide Abstract
The genome sequence of Nobel Laureate Dr. James D. Watson was determined using 454 sequencing technology at a 6x coverage. The sequence was matched to the human genome project's published reference sequence to guide assembly into gene-length pieces. The entire Watson sequence, with one exception, has been publicly released in NCBI's Trace Archive and the Cold Spring Harbor Laboratories web site. The sequence of the ApoE gene, variants of which are associated with early-onset Alzheimer's Disease, was not released. The sequence data is available in NCBI's Trace database and can be downloaded from the TraceDB FTP Site. Those sequences that are not present in the human reference sequence were assembled into an accessioned WGS project (ABKV01000000). The last two contigs (ABKV01169335 and ABKV01169336) are mitochondrial sequences.
Sample: Generic sample from Homo sapiens
SAMN00001698 • SRS000284 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: L1
Instrument: 454 GS FLX
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: SINGLE
Spot descriptor:
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Runs: 8 runs, 1.2M spots, 316.3M bases, 754.8Mb
Run# of Spots# of BasesSizePublished
SRR000416167,21245.7M109Mb2007-06-05
SRR000440142,00638.9M93Mb2007-06-05
SRR000445109,49830.4M73Mb2007-06-05
SRR000481132,41136M85.9Mb2007-06-05
SRR000509165,66145M107.3Mb2007-06-05
SRR000533155,11342.6M101.4Mb2007-06-05
SRR000549101,75727.9M67.6Mb2007-06-05
SRR000550181,00149.8M117.6Mb2007-06-05

ID:
114

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