dna sequence data files Search Results


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DNA Link Inc genome sequencing raw data pacbio
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Guangzhou Kingmed Diagnostics Group Co Ltd dna sequence data
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dna Sequence Data, supplied by Guangzhou Kingmed Diagnostics Group Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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WholeGenome LLC genomic dna sequence
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Genomic Dna Sequence, supplied by WholeGenome LLC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Centogene GmbH dna extraction, sequencing, and data analysis (bioinformatics and quality control processes)
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dna Extraction, Sequencing, And Data Analysis (Bioinformatics And Quality Control Processes), supplied by Centogene GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dna extraction, sequencing, and data analysis (bioinformatics and quality control processes) - by Bioz Stars, 2026-06
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CodonCode corporation dna sequence files
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dna Sequence Files, supplied by CodonCode corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Broad Institute Inc dna sequencing, mrna sequencing, dna copy number alteration, and clinical data
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dna Sequencing, Mrna Sequencing, Dna Copy Number Alteration, And Clinical Data, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dna sequencing, mrna sequencing, dna copy number alteration, and clinical data - by Bioz Stars, 2026-06
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CH Instruments dna sequence data
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dna Sequence Data, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Active Motif dna sequencing, computational, and statistical analyses of chip-seq data
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dna Sequencing, Computational, And Statistical Analyses Of Chip Seq Data, supplied by Active Motif, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dna sequencing, computational, and statistical analyses of chip-seq data - by Bioz Stars, 2026-06
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Federation of European Neuroscience Societies dendrograms of mlst data and dna repair component sequences
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dendrograms Of Mlst Data And Dna Repair Component Sequences, supplied by Federation of European Neuroscience Societies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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dendrograms of mlst data and dna repair component sequences - by Bioz Stars, 2026-06
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LGC Genomics GmbH dna sequence data
A RB1 mutation rates by <t>DNA</t> sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), <t>and</t> <t>ALS</t> (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).
Dna Sequence Data, supplied by LGC Genomics GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Ginkgo Bioworks dna sequencing data
Results of searching for exact matches to gRNA DNA sequences in available raw <t> DNAseq </t> data for circuit strains. A cell contains 0 if its column gRNA DNA sequence is absent from its row circuit strain, and it contains 1 if its column gRNA DNA sequence is present in its row circuit strain. A cell is colored orange or blue if the absence or presence, respectively, of its column gRNA DNA sequence is unexpected based on the design of its row circuit strain. An unexpected absence of a gRNA DNA sequence may be due to an error in building a circuit strain or poor <t> DNAseq </t> coverage, while an unexpected presence of a gRNA DNA sequence may be due to a mislabeled sample, an inaccurate design specification for a circuit strain or contamination of <t> sequencing </t> data for one strain with another.
Dna Sequencing Data, supplied by Ginkgo Bioworks, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


A RB1 mutation rates by DNA sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), and ALS (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).

Journal: Cell Death Discovery

Article Title: Role of RB1 in neurodegenerative diseases: inhibition of post-mitotic neuronal apoptosis via Kmt5b

doi: 10.1038/s41420-024-01955-y

Figure Lengend Snippet: A RB1 mutation rates by DNA sequence data in blood samples from PD (n = 189), AD (n = 33), HD (n = 69), and ALS (n = 75) patients from the Guangzhou KingMed Diagnostics Group Co. B Detailed information of the six mutation sites in neurodegenerative patients. C The detailed frequencies of the six mutation sites in neurodegenerative patients, normal Eastern Asian population, and frequency in the ALAF project from NCBI. PD Parkinson’s disease, AD Alzheimer’s disease, HD Huntington’s disease, ALS amyotrophic lateral sclerosis; -: no data. (Fisher’s exact test; *** P < 0.001).

Article Snippet: To determine the relationship between RB1 mutations and neurodegenerative disease, we calculated the RB1 mutation rates of PD (189 blood samples), AD (33 blood samples), HD (69 blood samples), and ALS (75 blood samples) using DNA sequence data from Guangzhou KingMed Diagnostics Group Co., Ltd.

Techniques: Mutagenesis, Sequencing

Results of searching for exact matches to gRNA DNA sequences in available raw  DNAseq  data for circuit strains. A cell contains 0 if its column gRNA DNA sequence is absent from its row circuit strain, and it contains 1 if its column gRNA DNA sequence is present in its row circuit strain. A cell is colored orange or blue if the absence or presence, respectively, of its column gRNA DNA sequence is unexpected based on the design of its row circuit strain. An unexpected absence of a gRNA DNA sequence may be due to an error in building a circuit strain or poor  DNAseq  coverage, while an unexpected presence of a gRNA DNA sequence may be due to a mislabeled sample, an inaccurate design specification for a circuit strain or contamination of  sequencing  data for one strain with another.

Journal: Synthetic Biology

Article Title: Highly-automated, high-throughput replication of yeast-based logic circuit design assessments

doi: 10.1093/synbio/ysac018

Figure Lengend Snippet: Results of searching for exact matches to gRNA DNA sequences in available raw DNAseq data for circuit strains. A cell contains 0 if its column gRNA DNA sequence is absent from its row circuit strain, and it contains 1 if its column gRNA DNA sequence is present in its row circuit strain. A cell is colored orange or blue if the absence or presence, respectively, of its column gRNA DNA sequence is unexpected based on the design of its row circuit strain. An unexpected absence of a gRNA DNA sequence may be due to an error in building a circuit strain or poor DNAseq coverage, while an unexpected presence of a gRNA DNA sequence may be due to a mislabeled sample, an inaccurate design specification for a circuit strain or contamination of sequencing data for one strain with another.

Article Snippet: The exception is the DNA sequencing (DNAseq) data, which were collected at Ginkgo Bioworks.

Techniques: Sequencing

SRA Metadata analysis of our DNAseq data. Sequence elements identified as missing plotted against estimated sequence coverage.

Journal: Synthetic Biology

Article Title: Highly-automated, high-throughput replication of yeast-based logic circuit design assessments

doi: 10.1093/synbio/ysac018

Figure Lengend Snippet: SRA Metadata analysis of our DNAseq data. Sequence elements identified as missing plotted against estimated sequence coverage.

Article Snippet: The exception is the DNA sequencing (DNAseq) data, which were collected at Ginkgo Bioworks.

Techniques: Sequencing