The efficiency of pooling in the detection of rare mutations [2]

American Journal of Human Genetics

Volumn 67, Issue 4, 2000, Pages 1036-1039

  Gastwirth, J L ^a  

^a NATIONAL CANCER INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL PROTOCOL; DIAGNOSTIC ACCURACY; GENE MUTATION; GENE POOL; HUMAN; LETTER; PRIORITY JOURNAL; SCREENING TEST;

EID: 0033794983     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/303097     Document Type: Letter

References (12)

1. DNA pooling in mutation detection with reference to sequence analysis
2. Analysis of multistage pooling studies of biological specimens for estimating disease incidence and prevalence
3. The detection of defective members of large populations
4. Estimation of the prevalence of a rare disease preserving the anonymity of the subjects by group testing: Application to estimating the prevalence of AIDS antibodies in blood donors
5. Screening with cost-effective quality control: Potential applications to HIV and drug testing
6. The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews
7. A two-stage adaptive group-testing procedure for estimating small proportions
8. Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: Application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulin-dependent diabetes
9. Pooled-sample testing as a herd screening tool for detection of bovine viral diarrhea virus in persistently infected cattle
10. Group testing with a new goal, estimation
11. On the informativeness and accuracy of pooled testing in estimating prevalence of a rare disease: Application to HIV screening
12. An efficient protocol for rare mutation genotyping in a large population