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SRX9500594: Methylome capture of HG003 using EMSeq with 100ng of input DNA
1 ILLUMINA (Illumina NovaSeq 6000) run: 197.3M spots, 59.6G bases, 23.2Gb downloads

Design: 100, 50 and 10 ng of genomic DNA spiked in with 2 ng unmethylated lambda and 0.1 ng CpG methylated pUC19 was fragmented to 500 bp (Covaris S2, 200 cycles per burst, 10% duty-cycle, intensity of 5 and treatment time of 50 seconds). EM-seq libraries were prepared using the NEBNext Enzymatic Methyl-seq (E7120, NEB) kit following manufacturers instructions. Final libraries were amplified with the included NEBNext Q5U polymerase using 4 cycles for 100 ng, 5 cycles for 50 ng and 7 cycles for 10 ng inputs.
Submitted by: Weill Cornell Medicine
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:
SAMN16727314 • SRS7709450 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: EMSeq_HG003_LAB01_REP01_100ng_1
Instrument: Illumina NovaSeq 6000
Strategy: Bisulfite-Seq
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Runs: 1 run, 197.3M spots, 59.6G bases, 23.2Gb
Run# of Spots# of BasesSizePublished
SRR13051138197,292,06759.6G23.2Gb2020-11-13

ID:
12416062

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