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Genotyping, sequencing and analysis of 140,000 adults from Mexico City

The Mexico City Prospective Study is a prospective cohort of more than 150,000 adults recruited two decades ago from the urban districts of Coyoacán and Iztapalapa in Mexico City(1). Here we generated genotype and exome-sequencing data for all individuals and whole-genome sequencing data for 9,950 s...

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Autores principales: Ziyatdinov, Andrey, Torres, Jason, Alegre-Díaz, Jesús, Backman, Joshua, Mbatchou, Joelle, Turner, Michael, Gaynor, Sheila M., Joseph, Tyler, Zou, Yuxin, Liu, Daren, Wade, Rachel, Staples, Jeffrey, Panea, Razvan, Popov, Alex, Bai, Xiaodong, Balasubramanian, Suganthi, Habegger, Lukas, Lanche, Rouel, Lopez, Alex, Maxwell, Evan, Jones, Marcus, García-Ortiz, Humberto, Ramirez-Reyes, Raul, Santacruz-Benítez, Rogelio, Nag, Abhishek, Smith, Katherine R., Damask, Amy, Lin, Nan, Paulding, Charles, Reppell, Mark, Zöllner, Sebastian, Jorgenson, Eric, Salerno, William, Petrovski, Slavé, Overton, John, Reid, Jeffrey, Thornton, Timothy A., Abecasis, Gonçalo, Berumen, Jaime, Orozco-Orozco, Lorena, Collins, Rory, Baras, Aris, Hill, Michael R., Emberson, Jonathan R., Marchini, Jonathan, Kuri-Morales, Pablo, Tapia-Conyer, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600010/
https://www.ncbi.nlm.nih.gov/pubmed/37821707
http://dx.doi.org/10.1038/s41586-023-06595-3
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author Ziyatdinov, Andrey
Torres, Jason
Alegre-Díaz, Jesús
Backman, Joshua
Mbatchou, Joelle
Turner, Michael
Gaynor, Sheila M.
Joseph, Tyler
Zou, Yuxin
Liu, Daren
Wade, Rachel
Staples, Jeffrey
Panea, Razvan
Popov, Alex
Bai, Xiaodong
Balasubramanian, Suganthi
Habegger, Lukas
Lanche, Rouel
Lopez, Alex
Maxwell, Evan
Jones, Marcus
García-Ortiz, Humberto
Ramirez-Reyes, Raul
Santacruz-Benítez, Rogelio
Nag, Abhishek
Smith, Katherine R.
Damask, Amy
Lin, Nan
Paulding, Charles
Reppell, Mark
Zöllner, Sebastian
Jorgenson, Eric
Salerno, William
Petrovski, Slavé
Overton, John
Reid, Jeffrey
Thornton, Timothy A.
Abecasis, Gonçalo
Berumen, Jaime
Orozco-Orozco, Lorena
Collins, Rory
Baras, Aris
Hill, Michael R.
Emberson, Jonathan R.
Marchini, Jonathan
Kuri-Morales, Pablo
Tapia-Conyer, Roberto
author_facet Ziyatdinov, Andrey
Torres, Jason
Alegre-Díaz, Jesús
Backman, Joshua
Mbatchou, Joelle
Turner, Michael
Gaynor, Sheila M.
Joseph, Tyler
Zou, Yuxin
Liu, Daren
Wade, Rachel
Staples, Jeffrey
Panea, Razvan
Popov, Alex
Bai, Xiaodong
Balasubramanian, Suganthi
Habegger, Lukas
Lanche, Rouel
Lopez, Alex
Maxwell, Evan
Jones, Marcus
García-Ortiz, Humberto
Ramirez-Reyes, Raul
Santacruz-Benítez, Rogelio
Nag, Abhishek
Smith, Katherine R.
Damask, Amy
Lin, Nan
Paulding, Charles
Reppell, Mark
Zöllner, Sebastian
Jorgenson, Eric
Salerno, William
Petrovski, Slavé
Overton, John
Reid, Jeffrey
Thornton, Timothy A.
Abecasis, Gonçalo
Berumen, Jaime
Orozco-Orozco, Lorena
Collins, Rory
Baras, Aris
Hill, Michael R.
Emberson, Jonathan R.
Marchini, Jonathan
Kuri-Morales, Pablo
Tapia-Conyer, Roberto
author_sort Ziyatdinov, Andrey
collection PubMed
description The Mexico City Prospective Study is a prospective cohort of more than 150,000 adults recruited two decades ago from the urban districts of Coyoacán and Iztapalapa in Mexico City(1). Here we generated genotype and exome-sequencing data for all individuals and whole-genome sequencing data for 9,950 selected individuals. We describe high levels of relatedness and substantial heterogeneity in ancestry composition across individuals. Most sequenced individuals had admixed Indigenous American, European and African ancestry, with extensive admixture from Indigenous populations in central, southern and southeastern Mexico. Indigenous Mexican segments of the genome had lower levels of coding variation but an excess of homozygous loss-of-function variants compared with segments of African and European origin. We estimated ancestry-specific allele frequencies at 142 million genomic variants, with an effective sample size of 91,856 for Indigenous Mexican ancestry at exome variants, all available through a public browser. Using whole-genome sequencing, we developed an imputation reference panel that outperforms existing panels at common variants in individuals with high proportions of central, southern and southeastern Indigenous Mexican ancestry. Our work illustrates the value of genetic studies in diverse populations and provides foundational imputation and allele frequency resources for future genetic studies in Mexico and in the United States, where the Hispanic/Latino population is predominantly of Mexican descent.
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spelling pubmed-106000102023-10-27 Genotyping, sequencing and analysis of 140,000 adults from Mexico City Ziyatdinov, Andrey Torres, Jason Alegre-Díaz, Jesús Backman, Joshua Mbatchou, Joelle Turner, Michael Gaynor, Sheila M. Joseph, Tyler Zou, Yuxin Liu, Daren Wade, Rachel Staples, Jeffrey Panea, Razvan Popov, Alex Bai, Xiaodong Balasubramanian, Suganthi Habegger, Lukas Lanche, Rouel Lopez, Alex Maxwell, Evan Jones, Marcus García-Ortiz, Humberto Ramirez-Reyes, Raul Santacruz-Benítez, Rogelio Nag, Abhishek Smith, Katherine R. Damask, Amy Lin, Nan Paulding, Charles Reppell, Mark Zöllner, Sebastian Jorgenson, Eric Salerno, William Petrovski, Slavé Overton, John Reid, Jeffrey Thornton, Timothy A. Abecasis, Gonçalo Berumen, Jaime Orozco-Orozco, Lorena Collins, Rory Baras, Aris Hill, Michael R. Emberson, Jonathan R. Marchini, Jonathan Kuri-Morales, Pablo Tapia-Conyer, Roberto Nature Article The Mexico City Prospective Study is a prospective cohort of more than 150,000 adults recruited two decades ago from the urban districts of Coyoacán and Iztapalapa in Mexico City(1). Here we generated genotype and exome-sequencing data for all individuals and whole-genome sequencing data for 9,950 selected individuals. We describe high levels of relatedness and substantial heterogeneity in ancestry composition across individuals. Most sequenced individuals had admixed Indigenous American, European and African ancestry, with extensive admixture from Indigenous populations in central, southern and southeastern Mexico. Indigenous Mexican segments of the genome had lower levels of coding variation but an excess of homozygous loss-of-function variants compared with segments of African and European origin. We estimated ancestry-specific allele frequencies at 142 million genomic variants, with an effective sample size of 91,856 for Indigenous Mexican ancestry at exome variants, all available through a public browser. Using whole-genome sequencing, we developed an imputation reference panel that outperforms existing panels at common variants in individuals with high proportions of central, southern and southeastern Indigenous Mexican ancestry. Our work illustrates the value of genetic studies in diverse populations and provides foundational imputation and allele frequency resources for future genetic studies in Mexico and in the United States, where the Hispanic/Latino population is predominantly of Mexican descent. Nature Publishing Group UK 2023-10-11 2023 /pmc/articles/PMC10600010/ /pubmed/37821707 http://dx.doi.org/10.1038/s41586-023-06595-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ziyatdinov, Andrey
Torres, Jason
Alegre-Díaz, Jesús
Backman, Joshua
Mbatchou, Joelle
Turner, Michael
Gaynor, Sheila M.
Joseph, Tyler
Zou, Yuxin
Liu, Daren
Wade, Rachel
Staples, Jeffrey
Panea, Razvan
Popov, Alex
Bai, Xiaodong
Balasubramanian, Suganthi
Habegger, Lukas
Lanche, Rouel
Lopez, Alex
Maxwell, Evan
Jones, Marcus
García-Ortiz, Humberto
Ramirez-Reyes, Raul
Santacruz-Benítez, Rogelio
Nag, Abhishek
Smith, Katherine R.
Damask, Amy
Lin, Nan
Paulding, Charles
Reppell, Mark
Zöllner, Sebastian
Jorgenson, Eric
Salerno, William
Petrovski, Slavé
Overton, John
Reid, Jeffrey
Thornton, Timothy A.
Abecasis, Gonçalo
Berumen, Jaime
Orozco-Orozco, Lorena
Collins, Rory
Baras, Aris
Hill, Michael R.
Emberson, Jonathan R.
Marchini, Jonathan
Kuri-Morales, Pablo
Tapia-Conyer, Roberto
Genotyping, sequencing and analysis of 140,000 adults from Mexico City
title Genotyping, sequencing and analysis of 140,000 adults from Mexico City
title_full Genotyping, sequencing and analysis of 140,000 adults from Mexico City
title_fullStr Genotyping, sequencing and analysis of 140,000 adults from Mexico City
title_full_unstemmed Genotyping, sequencing and analysis of 140,000 adults from Mexico City
title_short Genotyping, sequencing and analysis of 140,000 adults from Mexico City
title_sort genotyping, sequencing and analysis of 140,000 adults from mexico city
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600010/
https://www.ncbi.nlm.nih.gov/pubmed/37821707
http://dx.doi.org/10.1038/s41586-023-06595-3
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