An approach to high-throughput genotyping.

[1]  Cécile Fizames,et al.  A comprehensive genetic map of the human genome based on 5,264 microsatellites , 1996, Nature.

[2]  K. Klinger,et al.  A simplified procedure for developing multiplex PCRs. , 1995, Genome research.

[3]  R. Elston,et al.  Two‐stage global search designs for linkage analysis using pairs of affected relatives , 1996 .

[4]  K H Buetow,et al.  A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC). , 1994, Science.

[5]  R. Mathies,et al.  Energy transfer primers: A new fluorescence labeling paradigm for DNA sequencing and analysis , 1996, Nature Medicine.

[6]  A. Jeffreys,et al.  Minisatellite variant repeat (MVR) mapping: analysis of 'null' repeat units at D1S8. , 1992, Human molecular genetics.

[7]  J. Weissenbach,et al.  A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish , 1996, Nature Genetics.

[8]  James B. Golden,et al.  Pattern Recognition for Automated DNA Sequencing: I. On-Line Signal Conditioning and Feature Extraction for Basecalling , 1993, ISMB.

[9]  H. Hayatsu,et al.  Reaction of sodium hypochlorite with nucleic acids and their constituents. , 1971, Chemical & pharmaceutical bulletin.

[10]  R. Richards,et al.  Incidence and origin of "null" alleles in the (AC)n microsatellite markers. , 1993, American journal of human genetics.

[11]  Eric S. Lander,et al.  A comprehensive genetic map of the mouse genome , 1996, Nature.

[12]  X. Cui,et al.  Multiplex genotype determination at a large number of gene loci. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[13]  J. Craig Venter,et al.  A model for high-throughput automated DNA sequencing and analysis core facilities , 1994, Nature.

[14]  M W Perlin,et al.  Toward fully automated genotyping: genotyping microsatellite markers by deconvolution. , 1995, American journal of human genetics.

[15]  R W Cottingham,et al.  Error detection for genetic data, using likelihood methods. , 1996, American journal of human genetics.

[16]  D. Botstein,et al.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms. , 1980, American journal of human genetics.

[17]  José Costa,et al.  PicoGreen quantitation of DNA: effective evaluation of samples pre- or post-PCR , 1996, Nucleic Acids Res..

[18]  D E Weeks,et al.  Polygenic disease: methods for mapping complex disease traits. , 1995, Trends in genetics : TIG.

[19]  D. Nickerson,et al.  Finnish-type aspartylglucosaminuria detected by oligonucleotide ligation assay. , 1995, Clinical chemistry.

[20]  G. Sensabaugh,et al.  Rapid sizing of short tandem repeat alleles using capillary array electrophoresis and energy-transfer fluorescent primers. , 1995, Analytical chemistry.

[21]  S. P. Fodor,et al.  Multiplexed biochemical assays with biological chips , 1993, Nature.

[22]  G. Gyapay,et al.  Correction of some genotyping errors in automated fluorescent microsatellite analysis by enzymatic removal of one base overhangs. , 1996, Nucleic acids research.

[23]  J. Carpten,et al.  Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping. , 1996, BioTechniques.

[24]  R. Fleischmann,et al.  Whole-genome random sequencing and assembly of Haemophilus influenzae Rd. , 1995, Science.

[25]  S. C. Jenkins,et al.  Chromosome–specific microsatellite sets for fluorescence–based, semi–automated genome mapping , 1994, Nature Genetics.

[26]  J. Hartley,et al.  Use of uracil DNA glycosylase to control carry-over contamination in polymerase chain reactions. , 1990, Gene.

[27]  J. Riley,et al.  Highly polymorphic minisatellite sequences: allele frequencies and mutation rates for five locus-specific probes in a Caucasian population. , 1990, Journal - Forensic Science Society.

[28]  S. Kwok,et al.  Avoiding false positives with PCR , 1989, Nature.

[29]  J. Witte,et al.  Genetic dissection of complex traits. , 1994, Nature genetics.

[30]  R A McIndoe,et al.  Single-tube genomic DNA isolation from whole blood without pre-isolating white blood cells. , 1995, BioTechniques.