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STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science

Short tandem repeats (STRs) are short repeated sequences commonly found in the human genome and valuable in forensic science, used for human identity and relatedness markers. Next-generation sequencing (NGS) technologies, e.g., ForenSeq Signature Prep, can sequence STRs, inferring length-based allel...

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Autores principales: Kulthammanit, Nuttachai, Sathirapatya, Tikumphorn, Sukawutthiya, Poonyapat, Noh, Hasnee, Vongpaisarnsin, Kornkiat, Wichadakul, Duangdao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351723/
https://www.ncbi.nlm.nih.gov/pubmed/37459339
http://dx.doi.org/10.1371/journal.pone.0282551
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author Kulthammanit, Nuttachai
Sathirapatya, Tikumphorn
Sukawutthiya, Poonyapat
Noh, Hasnee
Vongpaisarnsin, Kornkiat
Wichadakul, Duangdao
author_facet Kulthammanit, Nuttachai
Sathirapatya, Tikumphorn
Sukawutthiya, Poonyapat
Noh, Hasnee
Vongpaisarnsin, Kornkiat
Wichadakul, Duangdao
author_sort Kulthammanit, Nuttachai
collection PubMed
description Short tandem repeats (STRs) are short repeated sequences commonly found in the human genome and valuable in forensic science, used for human identity and relatedness markers. Next-generation sequencing (NGS) technologies, e.g., ForenSeq Signature Prep, can sequence STRs, inferring length-based alleles and single nucleotide polymorphisms (SNPs) and providing valuable insights into population and sub-population structures. Despite the potential benefits of NGS for STRs, no open-source software platform integrates the collection, management, and analysis of STR data from NGS into one place. Users must use multiple programs to process their STR data and then collect the results into a separate database or a file system folder. Moreover, analyzing repeat structures (STR repeat motifs) may require learning multiple software tools, making the process inefficient and cumbersome. To address this gap, we introduce the STRategy, a standalone web-based application supporting essential STR data management and analysis capabilities. The STRategy allows users to collect their data into its database, automatically calculates forensic parameters, and visualizes the analyzed data in various forms. Users can search the database using different options, such as by profile, loci, and genotypes, with and without a specific test kit. Moreover, users can also find the nucleotide variants of a locus among the samples. We designed the STRategy for internal use in a laboratory or an organization. Hence, our system includes role-based access control that allows users to search for or access specific data based on their responsibilities. The administrator role can customize the system, for example, configure maps according to the samples’ geographic data, and manage reference STR repeat motifs. A laboratory or an organization can download and install a copy of STRategy on their local system using Docker, as described in https://github.com/cucpbioinfo/STRategy. In summary, the STRategy is an end-to-end system that provides users with a database to collect the analyzed STR data from NGS, the dynamic analyses of forensic parameters, and the variants of STR patterns according to the newly added samples, which are then explorable via various search options and visualizations. The system is helpful for both forensic investigations and forensic genetics.
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spelling pubmed-103517232023-07-18 STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science Kulthammanit, Nuttachai Sathirapatya, Tikumphorn Sukawutthiya, Poonyapat Noh, Hasnee Vongpaisarnsin, Kornkiat Wichadakul, Duangdao PLoS One Research Article Short tandem repeats (STRs) are short repeated sequences commonly found in the human genome and valuable in forensic science, used for human identity and relatedness markers. Next-generation sequencing (NGS) technologies, e.g., ForenSeq Signature Prep, can sequence STRs, inferring length-based alleles and single nucleotide polymorphisms (SNPs) and providing valuable insights into population and sub-population structures. Despite the potential benefits of NGS for STRs, no open-source software platform integrates the collection, management, and analysis of STR data from NGS into one place. Users must use multiple programs to process their STR data and then collect the results into a separate database or a file system folder. Moreover, analyzing repeat structures (STR repeat motifs) may require learning multiple software tools, making the process inefficient and cumbersome. To address this gap, we introduce the STRategy, a standalone web-based application supporting essential STR data management and analysis capabilities. The STRategy allows users to collect their data into its database, automatically calculates forensic parameters, and visualizes the analyzed data in various forms. Users can search the database using different options, such as by profile, loci, and genotypes, with and without a specific test kit. Moreover, users can also find the nucleotide variants of a locus among the samples. We designed the STRategy for internal use in a laboratory or an organization. Hence, our system includes role-based access control that allows users to search for or access specific data based on their responsibilities. The administrator role can customize the system, for example, configure maps according to the samples’ geographic data, and manage reference STR repeat motifs. A laboratory or an organization can download and install a copy of STRategy on their local system using Docker, as described in https://github.com/cucpbioinfo/STRategy. In summary, the STRategy is an end-to-end system that provides users with a database to collect the analyzed STR data from NGS, the dynamic analyses of forensic parameters, and the variants of STR patterns according to the newly added samples, which are then explorable via various search options and visualizations. The system is helpful for both forensic investigations and forensic genetics. Public Library of Science 2023-07-17 /pmc/articles/PMC10351723/ /pubmed/37459339 http://dx.doi.org/10.1371/journal.pone.0282551 Text en © 2023 Kulthammanit et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kulthammanit, Nuttachai
Sathirapatya, Tikumphorn
Sukawutthiya, Poonyapat
Noh, Hasnee
Vongpaisarnsin, Kornkiat
Wichadakul, Duangdao
STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science
title STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science
title_full STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science
title_fullStr STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science
title_full_unstemmed STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science
title_short STRategy: A support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science
title_sort strategy: a support system for collecting and analyzing next-generation sequencing data of short tandem repeats for forensic science
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351723/
https://www.ncbi.nlm.nih.gov/pubmed/37459339
http://dx.doi.org/10.1371/journal.pone.0282551
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