Marth et al., 2003 - Google Patents
Sequence variations in the public human genome data reflect a bottlenecked population historyMarth et al., 2003
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- 5857865341973744355
- Author
- Marth G
- Schuler G
- Yeh R
- Davenport R
- Agarwala R
- Church D
- Wheelan S
- Baker J
- Ward M
- Kholodov M
- Phan L
- Czabarka E
- Murvai J
- Cutler D
- Wooding S
- Rogers A
- Chakravarti A
- Harpending H
- Kwok P
- Sherry S
- Publication year
- Publication venue
- Proceedings of the National Academy of Sciences
External Links
Snippet
Single-nucleotide polymorphisms (SNPs) constitute the great majority of variations in the human genome, and as heritable variable landmarks they are useful markers for disease mapping and resolving population structure. Redundant coverage in overlaps of large-insert …
- 238000005215 recombination 0 abstract description 36
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- G06F19/00—Digital computing or data processing equipment or methods, specially adapted for specific applications
- G06F19/10—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology
- G06F19/18—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology for functional genomics or proteomics, e.g. genotype-phenotype associations, linkage disequilibrium, population genetics, binding site identification, mutagenesis, genotyping or genome annotation, protein-protein interactions or protein-nucleic acid interactions
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- G06—COMPUTING; CALCULATING; COUNTING
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- G06F19/28—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology for programming tools or database systems, e.g. ontologies, heterogeneous data integration, data warehousing or computing architectures
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- G06F19/22—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology for sequence comparison involving nucleotides or amino acids, e.g. homology search, motif or SNP [Single-Nucleotide Polymorphism] discovery or sequence alignment
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- G06F19/12—Bioinformatics, i.e. methods or systems for genetic or protein-related data processing in computational molecular biology for modelling or simulation in systems biology, e.g. probabilistic or dynamic models, gene-regulatory networks, protein interaction networks or metabolic networks
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