Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Inference of haplotypes from PCR-amplified samples of diploid populations.

Molecular biology and evolution - 1 Mar 1990

Clark A G

Abstract excerpt

Direct sequencing of genomic DNA from diploid individuals leads to ambiguities on sequencing gels whenever there is more than one mismatching site in the sequences of the two orthologous copies of a gene. While these ambiguities cannot be resolved from a single sample without resorting to other experimental methods (such as cloning in the traditional way), population samples may be useful for inferring...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Base Sequence
Share to DNA

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Drosophila melanogaster

Share to Haplotypes

Share to Models, Genetic

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 2108305
DOI: 10.1093/oxfordjournals.molbev.a040591

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inference of haplotypes from PCR-amplified samples of diploid populations.PMID 2108305Read ↗

The accuracy of heterozygous base calling from diploid sequence and resolution of haplotypes using allele-specific sequencing.Semantic proximity Read ↗

Estimating Allele Frequencies.Semantic proximity Read ↗

How to infer reliable diploid genotypes from NGS or traditional sequence data: from basic probability to experimental optimization.Semantic proximity Read ↗

Using Haplotype Information for Conservation Genomics.Semantic proximity Read ↗

SNPSTRs: empirically derived, rapidly typed, autosomal haplotypes for inference of population history and mutational processes.Semantic proximity Read ↗

Screening techniques for detecting allelic variation in DNA sequences.Semantic proximity Read ↗

Haplotyping by double PCR amplification of specific alleles.Semantic proximity Read ↗

Rapid surveying of DNA sequence variation in natural populations.Semantic proximity Read ↗

Inference of haplotypes from samples of diploid populations: complexity and algorithms.Semantic proximity Read ↗

Direct micro-haplotyping by multiple double PCR amplifications of specific alleles (MD-PASA).Semantic proximity Read ↗

Incorporating allelic variation for reconstructing the evolutionary history of organisms from multiple genes: An example from Rosa in North America.Semantic proximity Read ↗

Determining relative microsatellite allele frequencies in pooled DNA samples.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.