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Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA

Short tandem repeats (STRs) are highly abundant in the human genome, but existing approaches for accurate genotyping of STRs are limited. Here, we describe a protocol for duplex molecular inversion probes for high-throughput and cost-effective STR enrichment. We have successfully tested panels targe...

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Detalles Bibliográficos
Autores principales: Tao, Liming, Marx, Zipora, Raz, Ofir, Shapiro, Ehud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452885/
https://www.ncbi.nlm.nih.gov/pubmed/34585162
http://dx.doi.org/10.1016/j.xpro.2021.100828
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author Tao, Liming
Marx, Zipora
Raz, Ofir
Shapiro, Ehud
author_facet Tao, Liming
Marx, Zipora
Raz, Ofir
Shapiro, Ehud
author_sort Tao, Liming
collection PubMed
description Short tandem repeats (STRs) are highly abundant in the human genome, but existing approaches for accurate genotyping of STRs are limited. Here, we describe a protocol for duplex molecular inversion probes for high-throughput and cost-effective STR enrichment. We have successfully tested panels targeting as many as 50K STRs in several thousands of genomic samples (e.g., HeLa cells, Du145 cells, leukemia cells, melanoma cells). However, because the protocol is plate based, the sample size is limited to a few thousand. For complete details on the use and execution of this protocol, please refer to Tao et al. (2021).
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spelling pubmed-84528852021-09-27 Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA Tao, Liming Marx, Zipora Raz, Ofir Shapiro, Ehud STAR Protoc Protocol Short tandem repeats (STRs) are highly abundant in the human genome, but existing approaches for accurate genotyping of STRs are limited. Here, we describe a protocol for duplex molecular inversion probes for high-throughput and cost-effective STR enrichment. We have successfully tested panels targeting as many as 50K STRs in several thousands of genomic samples (e.g., HeLa cells, Du145 cells, leukemia cells, melanoma cells). However, because the protocol is plate based, the sample size is limited to a few thousand. For complete details on the use and execution of this protocol, please refer to Tao et al. (2021). Elsevier 2021-09-16 /pmc/articles/PMC8452885/ /pubmed/34585162 http://dx.doi.org/10.1016/j.xpro.2021.100828 Text en © 2021 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Tao, Liming
Marx, Zipora
Raz, Ofir
Shapiro, Ehud
Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA
title Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA
title_full Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA
title_fullStr Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA
title_full_unstemmed Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA
title_short Efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified DNA
title_sort efficient acquisition of tens of thousands of short tandem repeats in single-cell whole-genome-amplified dna
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452885/
https://www.ncbi.nlm.nih.gov/pubmed/34585162
http://dx.doi.org/10.1016/j.xpro.2021.100828
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