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SRX1497273: GIAB SOLiD 5500W: HG002_NA24385_son: Sample HG002
1 ABI_SOLID (AB 5500xl-W Genetic Analysis System) run: 4.7G spots, 353.7G bases, 223.1Gb downloads

Design: Design: Duplicate libraries were constructed from each of the first and last vials of the NIST Reference Material 8391, Human DNA for Whole-Genome Variant Assessment, components HG-002 and HG-005. Libraries W2F4 and W2L4 are from HG-002 and represent the first and last (10,728) vials, respectively, of the initial lot of material. Libraries W5A1 and W5F1 (10,329) are from HG-005 and represent the first and last vials, respectively, of the initial lot of material. Libraries were prepared manually for HG-002 with the Life Technologies 5500 SOLiD Fragment Library Core Kit (PN 4464412). For HG-005 libraries were prepared using the automated AB Library Builder System with the Life Technologies Library Builder Fragment Core Kit for 5500 Genetic Analysis Systems (PN 4463763). Library conversion for measurement on the Life Technologies 5500W Genetic Analyzer was completed using the Life Technologies 5500W Conversion Primers Kit (PN 4478020). Individual libraries were sequenced on individual lanes of a flowchip on a 5500W Genetic Analyzer. Sequencing the 5500W libraries was completed with 75 base single-end reads using the 5500W Forward SR 75 Reagent (PN 4475685). 24 lanes (4 Flowchips) per genome were sequenced. 5500W generated .xsq files were mapped to the hg19 assembly using Life Technologies LifeScope Software (version 2.5). Mapped data resulted in total coverage of 78.7X for HG-002 and 62.2X for HG-005. Mean mapped read lengths were 57 bases and 55 bases for HG-002 and HG-005, respectively. All .bam files for the individual genomes were merged. Vial and run information in maintained in the Read Groups.
Submitted by: NCBI
Study: A public-private-academic consortium, Genome-in-a-Bottle (GIAB), hosted by NIST to develop reference materials and standards for clinical sequencing
show Abstracthide Abstract
The Genome in a Bottle Consortium (www.genomeinabottle.org) is a collaboration between NIST, FDA, NCBI, other government agencies, academic sequencing groups, sequencing technology developers, and clinical laboratories. A principal motivation for this consortium is to develop widely accepted reference materials and accompanying performance metrics to provide a strong scientific foundation for the development of regulations and professional standards for clinical sequencing. NIST is developing large batches of human genome DNA from several cell lines for NIST Reference Materials (RMs), which will be characterized by the Consortium for homogeneity, stability, and sequence with as much sequencing technologies and library preparation methods as possible. Information from these datasets will be integrated to form a high-confidence set of genotype calls, which can be used by clinical and research laboratories to understand performance of their sequencing and bioinformatics methods. NCBI is serving as the DCC and repository for the raw sequencing reads, mapped reads, genotypes, and other details for each sample on a dedicated FTP site ( ftp://ftp-trace.ncbi.nih.gov/giab/ftp/ ). The pilot sample is NA12878 (HG001), and NIST received over 8,000 aliquots in April 2013, which will initially be distributed to partners in the Consortium to assist in characterization, and later will be distributed by NIST as Reference Material 8398, likely in March or April 2015. Samples from an Ashkenazim trio (son HG002-NA24385-huAA53E0, father HG003-NA24149-hu6E4515, and mother HG004-NA24143-hu8E87A9), and a Han Chinese trio (son HG005-NA24631-hu91BD69, father NA24694-huCA017E, and mother NA24695-hu38168C) from Personal Genome Project (PGP) are also candidate NIST reference materials and are currently being characterized. The Ashkenazim trio will be available both as NIST RMs 8391 (son only) and 8392 (entire trio). Only the son of the Asian trio will be a NIST RM (8393). DNA and cell lines for all samples are also available from Coriell, but the NIST RMs are from a single homogenized batch of DNA, so there may be small differences between the samples at Coriell and the NIST RMs. Details about the NIST Reference Materials, data, and future plans are at https://sites.stanford.edu/abms/content/giab-reference-materials-and-data. When the NIST RMs are available, they can be purchased from NIST at http://www.nist.gov/srm/, where a Report of Investigation describing the DNA will also be available.
Sample: NIST HG002 NA24385
SAMN03283347 • SRS817069 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: HG002_NA24385_son_NIST_SOLiD5500W
Instrument: AB 5500xl-W Genetic Analysis System
Strategy: WGS
Source: GENOMIC
Selection: size fractionation
Layout: SINGLE
Spot descriptor:
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Runs: 1 run, 4.7G spots, 353.7G bases, 223.1Gb
Run# of Spots# of BasesSizePublished
SRR30476324,716,205,303353.7G223.1Gb2015-12-24

ID:
2120286

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