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AScall – Automatic Allele-Specific qPCR Analysis

Minor histocompatibility antigens (MiHA) are critical elements for the immune response after allogeneic hematopoietic stem cell transplantation. They may cause both beneficial and detrimental effects in forms of graft-versus-tumor and graft-versus-host accordingly. MiHAs originate from donor-recipie...

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Autores principales: Blagodatskikh, Konstantin, Romaniuk, Dmitrii, Malko, Dmitry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188954/
https://www.ncbi.nlm.nih.gov/pubmed/32391349
http://dx.doi.org/10.3389/fbioe.2020.00353
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author Blagodatskikh, Konstantin
Romaniuk, Dmitrii
Malko, Dmitry
author_facet Blagodatskikh, Konstantin
Romaniuk, Dmitrii
Malko, Dmitry
author_sort Blagodatskikh, Konstantin
collection PubMed
description Minor histocompatibility antigens (MiHA) are critical elements for the immune response after allogeneic hematopoietic stem cell transplantation. They may cause both beneficial and detrimental effects in forms of graft-versus-tumor and graft-versus-host accordingly. MiHAs originate from donor-recipient discrepancies in single nucleotide polymorphisms, insertions, and deletions. To determine the genetic mismatches between a donor and a recipient, we have implemented a real-time PCR method in conjunction with allele-specific primers (AS-qPCR). The new approach allows for multiplexing up to 480 reactions per 96 well plate and differs from common qPCR based genotyping methods. Earlier, we have confirmed and published the AS-qPCR method, but standard software for qPCR analysis does not suit AS-qPCR data. Here we fill this gap and describe AScall – the interactive web application for the proposed genotyping method. With a convenient interface mimicking a regular qPCR machine interface, our tool allows batch qPCR data import via universal RDML format, amplification curves preprocessing, quality control, sample genotype calling, detailed results visualization, and report generation. We show the use of AScall for SNP and indel genotyping for the MiHA study, but anyone can use the application for an accordingly designed AS-qPCR experiment of their own. Genotyping was done manually and with AScall for 96 genomic DNA samples. AScall processed 4,800 qPCRs in 1.5 min, with only two genotype mismatches compared to manual analysis. It took 3 h for an experienced researcher for manual analysis. Source code is freely available for download at https://github.com/kablag/AScall. The tool is freely available on the web at the AScall server http://shtest.evrogen.net/AScall.
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spelling pubmed-71889542020-05-08 AScall – Automatic Allele-Specific qPCR Analysis Blagodatskikh, Konstantin Romaniuk, Dmitrii Malko, Dmitry Front Bioeng Biotechnol Bioengineering and Biotechnology Minor histocompatibility antigens (MiHA) are critical elements for the immune response after allogeneic hematopoietic stem cell transplantation. They may cause both beneficial and detrimental effects in forms of graft-versus-tumor and graft-versus-host accordingly. MiHAs originate from donor-recipient discrepancies in single nucleotide polymorphisms, insertions, and deletions. To determine the genetic mismatches between a donor and a recipient, we have implemented a real-time PCR method in conjunction with allele-specific primers (AS-qPCR). The new approach allows for multiplexing up to 480 reactions per 96 well plate and differs from common qPCR based genotyping methods. Earlier, we have confirmed and published the AS-qPCR method, but standard software for qPCR analysis does not suit AS-qPCR data. Here we fill this gap and describe AScall – the interactive web application for the proposed genotyping method. With a convenient interface mimicking a regular qPCR machine interface, our tool allows batch qPCR data import via universal RDML format, amplification curves preprocessing, quality control, sample genotype calling, detailed results visualization, and report generation. We show the use of AScall for SNP and indel genotyping for the MiHA study, but anyone can use the application for an accordingly designed AS-qPCR experiment of their own. Genotyping was done manually and with AScall for 96 genomic DNA samples. AScall processed 4,800 qPCRs in 1.5 min, with only two genotype mismatches compared to manual analysis. It took 3 h for an experienced researcher for manual analysis. Source code is freely available for download at https://github.com/kablag/AScall. The tool is freely available on the web at the AScall server http://shtest.evrogen.net/AScall. Frontiers Media S.A. 2020-04-22 /pmc/articles/PMC7188954/ /pubmed/32391349 http://dx.doi.org/10.3389/fbioe.2020.00353 Text en Copyright © 2020 Blagodatskikh, Romaniuk and Malko. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Blagodatskikh, Konstantin
Romaniuk, Dmitrii
Malko, Dmitry
AScall – Automatic Allele-Specific qPCR Analysis
title AScall – Automatic Allele-Specific qPCR Analysis
title_full AScall – Automatic Allele-Specific qPCR Analysis
title_fullStr AScall – Automatic Allele-Specific qPCR Analysis
title_full_unstemmed AScall – Automatic Allele-Specific qPCR Analysis
title_short AScall – Automatic Allele-Specific qPCR Analysis
title_sort ascall – automatic allele-specific qpcr analysis
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188954/
https://www.ncbi.nlm.nih.gov/pubmed/32391349
http://dx.doi.org/10.3389/fbioe.2020.00353
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