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A universal method for automated gene mapping
Small insertions or deletions (InDels) constitute a ubiquituous class of sequence polymorphisms found in eukaryotic genomes. Here, we present an automated high-throughput genotyping method that relies on the detection of fragment-length polymorphisms (FLPs) caused by InDels. The protocol utilizes st...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC551539/ https://www.ncbi.nlm.nih.gov/pubmed/15693948 http://dx.doi.org/10.1186/gb-2005-6-2-r19 |
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author | Zipperlen, Peder Nairz, Knud Rimann, Ivo Basler, Konrad Hafen, Ernst Hengartner, Michael Hajnal, Alex |
author_facet | Zipperlen, Peder Nairz, Knud Rimann, Ivo Basler, Konrad Hafen, Ernst Hengartner, Michael Hajnal, Alex |
author_sort | Zipperlen, Peder |
collection | PubMed |
description | Small insertions or deletions (InDels) constitute a ubiquituous class of sequence polymorphisms found in eukaryotic genomes. Here, we present an automated high-throughput genotyping method that relies on the detection of fragment-length polymorphisms (FLPs) caused by InDels. The protocol utilizes standard sequencers and genotyping software. We have established genome-wide FLP maps for both Caenorhabditis elegans and Drosophila melanogaster that facilitate genetic mapping with a minimum of manual input and at comparatively low cost. |
format | Text |
id | pubmed-551539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5515392005-03-03 A universal method for automated gene mapping Zipperlen, Peder Nairz, Knud Rimann, Ivo Basler, Konrad Hafen, Ernst Hengartner, Michael Hajnal, Alex Genome Biol Method Small insertions or deletions (InDels) constitute a ubiquituous class of sequence polymorphisms found in eukaryotic genomes. Here, we present an automated high-throughput genotyping method that relies on the detection of fragment-length polymorphisms (FLPs) caused by InDels. The protocol utilizes standard sequencers and genotyping software. We have established genome-wide FLP maps for both Caenorhabditis elegans and Drosophila melanogaster that facilitate genetic mapping with a minimum of manual input and at comparatively low cost. BioMed Central 2005 2005-01-17 /pmc/articles/PMC551539/ /pubmed/15693948 http://dx.doi.org/10.1186/gb-2005-6-2-r19 Text en Copyright © 2005 Zipperlen et al.; licensee BioMed Central Ltd. |
spellingShingle | Method Zipperlen, Peder Nairz, Knud Rimann, Ivo Basler, Konrad Hafen, Ernst Hengartner, Michael Hajnal, Alex A universal method for automated gene mapping |
title | A universal method for automated gene mapping |
title_full | A universal method for automated gene mapping |
title_fullStr | A universal method for automated gene mapping |
title_full_unstemmed | A universal method for automated gene mapping |
title_short | A universal method for automated gene mapping |
title_sort | universal method for automated gene mapping |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC551539/ https://www.ncbi.nlm.nih.gov/pubmed/15693948 http://dx.doi.org/10.1186/gb-2005-6-2-r19 |
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