Evidence map›Paper›PMID 12883999›Full record

ArticleHuman genetics2003

A novel method for automatic genotyping of microsatellite markers based on parametric pattern recognition.

Asa Johansson, Patrik Karlsson, Ulf Gyllensten

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Article in Human genetics, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Genetic Characterization ofJournal of fungi (Basel, Switzerland) · 2022
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Asa JohanssonDepartment of Genetics and Pathology, Rudbeck Laboratory, Uppsala University, 571 85, Uppsala, Sweden.
Patrik Karlsson
Ulf Gyllensten

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic mapping of loci affecting complex phenotypes in human and other organisms is presently being conducted on a very large scale, using either microsatellite or single nucleotide polymorphism (SNP) markers and by partly automated methods. A critical step in this process is the conversion of the instrument output into genotypes, both a time-consuming and error prone procedure. Errors made during this calling of genotypes will dramatically reduce the ability to map the location of loci underlying a phenotype. Accurate methods for automatic genotype calling are therefore important. Here, we describe novel algorithms for automatic calling of microsatellite genotypes using parametric pattern recognition. The analysis of microsatellite data is complicated both by the occurrence of stutter bands, which arise from Taq polymerase misreading the number of repeats, and additional bands derived form the non-template dependent addition of a nucleotide to the 3' end of the PCR products. These problems, together with the fact that the lengths of two alleles in a heterozygous individual may differ by only two nucleotides, complicate the development of an automated process. The novel algorithms markedly reduce the need for manual editing and the frequency of miscalls, and compares very favourably with commercially available software for automatic microsatellite genotyping.

Indexed as

Microsatellite RepeatsAlgorithmsAnimalsChromatographyChromosome MappingDatabases, GeneticGenetic MarkersHumansModels, GeneticGenetic Markers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.