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Biotechnology Information genomic sequence data
Genomic Sequence Data, supplied by Biotechnology Information, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/genome+sequencing+data/data+rna+seq+%E2%80%A2/pm42277643-384-1-15
Average 86 stars, based on 1 article reviews
genomic sequence data - by Bioz Stars, 2026-10
86/100 stars

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Sequencing:

Article Title: Inhibition of Growth and Biofilm Formation in Staphylococcus aureus by LLY-507
Article Snippet: .. The whole-genome sequencing data were deposited in the National Center for Biotechnology Information (NCBI) with accession number PRJNA1166673 (NCBI: http://www.ncbi.nlm.nih.gov/bioproject/1166673 ). .. The whole-genome sequencing data were deposited in the National Center for Biotechnology Information (NCBI) with accession number PRJNA1166673 (NCBI: http://www.ncbi.nlm.nih.gov/bioproject/1166673 ).

Article Title: Genomic analysis and antimicrobial resistance of Vibrio cholerae isolated during Zambia's 2023 cholera epidemic.
Article Snippet: .. All whole- genome sequencing data generated in the study are available in the National Center for Biotechnology Information under the accession number PRJNA1228025. ..

Article Title: Loss of the ferripyochelin receptor FptA drives reduced cefiderocol susceptibility and impairs fitness in Pseudomonas aeruginosa PA14.
Article Snippet: .. The whole genome sequencing data is available at the National Center for Biotechnology Information (NCBI) website, Bioproject accession number PRJNA1316631. ..

Article Title: Within-patient evolution of Pseudomonas aeruginosa populations during antimicrobial treatment.
Article Snippet: .. Genome sequencing data used in this study are available in the National Center for Biotechnology Information (NCBI) under BioProject PRJNA1332666, with accession information listed in Table S3. ..

Article Title: Biological valorization of methane and nitrogen gas-derived ammonia via methanotrophic bacteria for gut-beneficial nutrients.
Article Snippet: .. The whole genome sequencing data of M. sanxanigenens NG09 have been deposited in National Center for Biotechnology Information (NCBI) under accession code JBOBHP000000000 [https://www.ncbi.nlm.nih.gov/nuccore/JBOBHP000000000.1/]. ..

Article Title: Phenotypic and genomic characterization of NDM-producing Escherichia coli colonizing the pediatric gut in Shenzhen, China
Article Snippet: .. The whole-genome sequencing data for the 25 NDM-producing E. coli isolates described in this study have been deposited in the National Center for Biotechnology Information ( https://www.ncbi.nlm.nih.gov/sra/?term= ) under the following accession numbers: SAMN54299078 – SAMN54299099 , SAMN54249838 , SAMN54242561 , and SAMN54242562 . ..

Article Title: Within-patient evolution of Pseudomonas aeruginosa populations during antimicrobial treatment
Article Snippet: .. Genome sequencing data used in this study are available in the National Center for Biotechnology Information (NCBI) under BioProject PRJNA1332666 , with accession information listed in . ..

Article Title: Epidemiological and characteristic differences of hypervirulent and classical Klebsiella pneumoniae : a clinical and genomic study in Southern China during the COVID-19 pandemic
Article Snippet: .. All whole-genome sequencing data from the study are available in the National Center for Biotechnology Information (NCBI) under project accession number PRJNA1248222. ..

Generated:

Article Title: Genomic analysis and antimicrobial resistance of Vibrio cholerae isolated during Zambia's 2023 cholera epidemic.
Article Snippet: .. All whole- genome sequencing data generated in the study are available in the National Center for Biotechnology Information under the accession number PRJNA1228025. ..



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Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; <t>WGII,</t> <t>whole-genome</t> instability index;ll *, P < 0.05.
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Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

Journal: Molecular Cancer Research

Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing

doi: 10.1158/1541-7786.MCR-25-0616

Figure Lengend Snippet: Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

Article Snippet: We analyzed whole-genome sequencing data on 164 tumor–normal pairs from the Genomics England 100,000 Genomes Project, providing a comprehensive, high-resolution map of copy number alterations, structural variation, and key global genomic features, including mutational signatures, intratumor heterogeneity, and analysis of extrachromosomal DNA formation.

Techniques: Sampling, Variant Assay

Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

Journal: Molecular Cancer Research

Article Title: Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing

doi: 10.1158/1541-7786.MCR-25-0616

Figure Lengend Snippet: Summary of clinical correlations adjusted for sex, age of sampling, and stage. A, ChCC ( n = 61) and ( B ) pRCC ( n = 103). CN, copy number; MB, megabase; SNV, single-nucleotide variant; TCRA, T-cell receptor-α; WGII, whole-genome instability index;ll *, P < 0.05.

Article Snippet: To address this shortcoming, we report the analysis of whole-genome sequencing (WGS) data generated on tumor–normal (T/N) pairs from 164 patients recruited from NHS Genomic Medicine Centres (GMC) across England, as part of the Genomics England 100,000 Genomes Project (100kGP, RRID: SCR_010502; refs , ).

Techniques: Sampling, Variant Assay