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SRX20503464: GSM7426174: P06; Homo sapiens; Bisulfite-Seq
1 ILLUMINA (NextSeq 500) run: 81.1M spots, 6.1G bases, 2.4Gb downloads

Submitted by: NCBI (GEO)
Study: LABS: linear amplification-based bisulfite sequencing for ultrasensitive cancer detection from cell-free DNA
show Abstracthide Abstract
Methylation-based liquid biopsies show promise in detecting cancer from circulating cell-free DNA, but current limitations impede clinical application. Most assays necessitate substantial DNA inputs, posing challenges. Underrepresented tumor DNA fragments may go undetected during exponential amplification steps of traditional sequencing methods. Here we report LABS (Linear Amplification based Bisulfite Sequencing), enabling linear amplification of bisulfite-treated DNA fragments in a genome-wide, unbiased fashion, detecting cancer abnormalities with sub-nanogram inputs. Applying LABS to 100 patient samples revealed cancer-specific patterns, copy number alterations, and enhanced cancer detection accuracy by identifying tissue-of-origin and immune cell composition. Overall design: For method validation, we compared our LABS method with two commonly used commercial methods: EpiGnome and MethylC-seq. For clinical usage, we collected cfDNA samples from 50 CRC, 16 PDAC, and 34 control patients.
Sample: P06
SAMN35355125 • SRS17826402 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: NextSeq 500
Strategy: Bisulfite-Seq
Source: OTHER
Selection: RANDOM
Layout: SINGLE
Construction protocol: Plasma were separated from blood,then cfDNA were extracted from plasma using zymo research Quick-cfRNA Serum & Plasma, 1 ng cfDNA was used for library construction. Methylated adapters were added with the NEBNext DNA library prep kit. Libraries were bisulfite converted with the Zymo EZ DNA Methylation Lightning kit.
Experiment attributes:
GEO Accession: GSM7426174
Links:
Runs: 1 run, 81.1M spots, 6.1G bases, 2.4Gb
Run# of Spots# of BasesSizePublished
SRR2472558481,068,5786.1G2.4Gb2024-04-24

ID:
27927037

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