ID
45343
Descrição
Principal Investigator: Jay Shendure, PhD, University of Washington, Seattle, WA, USA MeSH: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000500 The overall purpose of this study was to demonstrate the feasibility of producing haplotype-phased whole genome sequence data from a fetus using free fetal DNA isolated from maternal plasma collected during the first half of gestation.
Link
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000500
Palavras-chave
Versões (2)
- 02/11/2022 02/11/2022 - Tabea Kampen
- 13/12/2022 13/12/2022 - Kristina Keller
Titular dos direitos
Jay Shendure, PhD, University of Washington, Seattle, WA, USA
Transferido a
2 de novembro de 2022
DOI
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Licença
Creative Commons BY 4.0
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dbGaP phs000500 Non-Invasive Whole Genome Sequencing of a Human Fetus
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent data table contains subject IDs, consent group information, subject ID aliases, and affection status.
- The pedigree data table contains pedigree and gender information of study participants. There are 2 family trios.
- The subject sample data table contains mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes a mapping of sample IDs to other sample ID aliases and sample use.
- The sample attributes data table includes body site where sample was extracted, sample analyte type and tumor status.
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Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent data table contains subject IDs, consent group information, subject ID aliases, and affection status.
- The pedigree data table contains pedigree and gender information of study participants. There are 2 family trios.
- The subject sample data table contains mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs. The data table also includes a mapping of sample IDs to other sample ID aliases and sample use.
- The sample attributes data table includes body site where sample was extracted, sample analyte type and tumor status.
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