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SRX2511758: Genome sequencing of synthetic Escherichia coli, C321.ĆA.740
1 ILLUMINA (Illumina HiSeq 2000) run: 186,369 spots, 56.1M bases, 14.6Mb downloads

Design: gDNA prep. cell culture was processed with a Qiagen DNeasy Blood and Tissue (cat: 69504) to extract genomic DNA. Sequencing. 2.5 g of gDNA was sent to the Yale Center Genome Analysis for library prep. One micrograms of gDNA were sheared to an expected size of 500 bases with Covaris E210 in a covaris microtube. Post-shearing cleanup was done with SPRI magnetic beads. ÔWith BeadŐ fragment end repair was performed with End Repair enzyme at 20űC for 30 min and purified. ÔWith beadŐ A-base addition was performed with A-Tailing enzyme at 30_C for 30 min and purified. Samples were barcoded with an adapter ligation mix. Ligation was purified. Samples were PCR enriched (26-l DNA; 30-l KAPA HiFi Mastermix; 2-ul 25-M PCR Primer MP1.0; 2-l 25-M barcode-specific primer). Samples were loaded onto a lane of an Illumina HiSeq 2000 for 76-base pairedend reads.
Submitted by: Northwestern University
Study: synthetic Escherichia coli C321.deltaA Genome sequencing
show Abstracthide Abstract
Here, we have sequenced the genomes of engineered strains of genomically recoded Escherichia coli lacking RF1 used to produce high yielding cell-free protein synthesis (CFPS) platform from crude extracts.
Sample: Escherichia coli C321.deltaA.740
SAMN06232395 • SRS1935451 • All experiments • All runs
Library:
Name: C321.ĆA.740
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: other
Layout: PAIRED
Runs: 1 run, 186,369 spots, 56.1M bases, 14.6Mb
Run# of Spots# of BasesSizePublished
SRR5196087186,36956.1M14.6Mb2017-01-24

ID:
3638132

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