A cSNP map and database for human chromosome 21

Genome Research

Volumn 11, Issue 2, 2001, Pages 300-307

  Deutsch, Samuel ^a   Iseli, Christian ^b,c   Bucher, Philipp ^c,d   Antonarakis, Stylianos E ^a   Scott, Hamish S ^a,e  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^b LUDWIG INSTITUTE FOR CANCER RESEARCH   (Switzerland)

^c SWISS INSTITUTE OF BIOINFORMATICS   (Switzerland)

^d SWISS INST FOR EXP CANCER RESEARCH   (Switzerland)

^e ROYAL MELBOURNE HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA;

ACCURACY; ALLELE; ARTICLE; CHROMOSOME 21; CHROMOSOME MAP; CONTROLLED STUDY; DATA BASE; DOWN SYNDROME; EXPRESSED SEQUENCE TAG; GENE LOCUS; GENE SEQUENCE; GENE TARGETING; GENETIC TRANSCRIPTION; HUMAN; INTERNET; MANIC DEPRESSIVE PSYCHOSIS; METHODOLOGY; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; VALIDATION PROCESS;

BASE COMPOSITION; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 21; DATABASES, FACTUAL; HUMANS; MOLECULAR SEQUENCE DATA; NUCLEOTIDES; POLYMORPHISM, SINGLE NUCLEOTIDE; REPRODUCIBILITY OF RESULTS; SEQUENCE ANALYSIS, DNA; VARIATION (GENETICS);

EID: 0035104666     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (33)

1. 10 years of genomics, chromosome 21, and Down syndrome
2. The essence of SNPs
3. Reliable identification of large numbers of candidate SNPs from public EST data
4. Sequence diversity in 36 candidate genes for cardiovascular disorders
5. Characterization of single-nucleotide polymorphisms in coding regions of human genes
6. Population genetics-Making sense out of sequence
7. Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase
8. Variations on a theme: Cataloging human DNA sequence variation
9. Gene conversion events contribute to the polymorphic variation of the surrogate light chain gene λ 5/14.1
10. Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain
11. Identification of candidate coding region single nucleotide polymorphisms in 165 human genes using assembled expressed sequence tags
12. Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
13. Archaic African and Asian lineages in the genetic ancestry of modern humans
14. The DNA sequence of human chromosome 21
15. Polymorphism of DNA sequence adjacent to human β-globin structural gene: Relationship to sickle mutation
16. Prospects for whole-genome linkage disequilibrium mapping of common disease genes
17. A 4-Mb high-density single nucleotide polymorphism-based map around human APOE
18. Identification of mutations in cystatin B, the gene responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy (EPM1)
19. Reading bits of genetic information: Methods for single-nucleotide polymorphism analysis
20. The new genomics: Global views of biology
21. Genetic dissection of complex traits
22. A general approach to single-nucleotide polymorphism discovery
23. Single nucleotide polymorphism and linkage disequilibrium within the TCR α/δ locus
24. DNA variability and recombination rates at X-linked loci in humans
25. Positional cloning of the APECED gene
26. Identification of 187 single nucleotide polymorphisms (SNPs) among 41 genes for ischemic heart disease in the Japanese population
27. Mining SNPs from EST database
28. The future of genetic studies of complex human diseases
29. Human genome research. SNP mappers confront reality and find it daunting
30. Detection of numerous Y chromosome biallelic polymorphisms by denaturing high-performance liquid chromatography
31. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
32. Identification of 142 single nucleotide polymorphisms in 41 candidate genes for rheumatoid arthritis in the Japanese population