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10X Genomics linked-read sequencing data
Linked Read Sequencing Data, supplied by 10X Genomics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/linked-reads+sequencing+data/linked+read+sequencing+data/pm38869148-295-12-10
Average 90 stars, based on 1 article reviews
linked-read sequencing data - by Bioz Stars, 2026-11
90/100 stars

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Related Articles

Mutagenesis:

Article Title: Low mutation rate in epaulette sharks is consistent with a slow rate of evolution in sharks
Article Snippet: .. Identification of de novo mutations To provide a direct estimate of the de novo mutation rate in the epaulette shark, we generated 10X Genomics linked-reads sequencing data for nine F1 progeny produced during our captive breeding experiment. ..

Generated:

Article Title: Low mutation rate in epaulette sharks is consistent with a slow rate of evolution in sharks
Article Snippet: .. Identification of de novo mutations To provide a direct estimate of the de novo mutation rate in the epaulette shark, we generated 10X Genomics linked-reads sequencing data for nine F1 progeny produced during our captive breeding experiment. ..

Sequencing:

Article Title: Low mutation rate in epaulette sharks is consistent with a slow rate of evolution in sharks
Article Snippet: .. Identification of de novo mutations To provide a direct estimate of the de novo mutation rate in the epaulette shark, we generated 10X Genomics linked-reads sequencing data for nine F1 progeny produced during our captive breeding experiment. ..

Article Title: LRTK: a platform agnostic toolkit for linked-read analysis of both human genome and metagenome.
Article Snippet: .. D1: The first real metagenomic dataset (D1), consisting of lonitudinal 10x Genomics linked-read sequencing data, was downoaded from the NCBI under accession number SRP323279. ..

Article Title: Hap10: reconstructing accurate and long polyploid haplotypes using linked reads
Article Snippet: .. Recently, 10X Genomics developed a linked-read sequencing library preparation strategy, commercialized through their Chromium platform, as a complementary technology to Illumina devices. ..

Article Title: Comprehensive identification of somatic nucleotide variants in human brain tissue
Article Snippet: .. We used haplotype information provided by 10X Genomics linked read sequencing data to eliminate false-positive mosaic SNV calls and to provide support for bona fide mosaic SNVs. .. Briefly, the 10X Genomics linked read approach is a barcoded short-read sequencing technology, where individual HMW genomic DNA molecules (~ 50 kb) initially are attached to a bead then incorporated into droplets.

Article Title: Rare transmission of commensal and pathogenic bacteria in the gut microbiome of hospitalized adults
Article Snippet: .. We prepared linked-read sequencing libraries with the 10X Genomics Chromium platform from 89 samples with sufficient DNA concentration. .. Samples were sequenced to a median of 116 million (M) (± 37 M SD) read pairs on an Illumina HiSeq4000.

Produced:

Article Title: Low mutation rate in epaulette sharks is consistent with a slow rate of evolution in sharks
Article Snippet: .. Identification of de novo mutations To provide a direct estimate of the de novo mutation rate in the epaulette shark, we generated 10X Genomics linked-reads sequencing data for nine F1 progeny produced during our captive breeding experiment. ..

other:

Article Title: Prediction of the 3D cancer genome from genomic rearrangements using InfoHiC
Article Snippet: SV calls of HCC1954 from linked-read sequencing data (10X Genomics) were downloaded from https://cf.10xgenomics.com/samples/genome/HCC1954TWGS210/HCC1954T_WGS_210_large_svs.vcf.gz .

Concentration Assay:

Article Title: Rare transmission of commensal and pathogenic bacteria in the gut microbiome of hospitalized adults
Article Snippet: .. We prepared linked-read sequencing libraries with the 10X Genomics Chromium platform from 89 samples with sufficient DNA concentration. .. Samples were sequenced to a median of 116 million (M) (± 37 M SD) read pairs on an Illumina HiSeq4000.



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