Long-Read Sequencing in Blood Group Genetics

被引:8
作者
Thun, Gian Andri [1 ]
Gueuning, Morgan [1 ]
Mattle-Greminger, Maja P. [1 ]
机构
[1] Swiss Red Cross, Dept Res & Dev, Blood Transfus Serv Zurich, Schlieren, Switzerland
关键词
Haplotype; Third-generation sequencing; Bloodgroupallele; Long-read sequencing; Structural variation; SINGLE-MOLECULE; DNA METHYLATION; PLATELET ANTIGENS; EVOLUTION; ALLELES; GENOME; GENES; CELL;
D O I
10.1159/000530652
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The key advantages of latest third-generation long-read sequencing (TGS) technologies include the ability to resolve long haplotypes and to characterize genomic regions that are challenging to analyze with short- read sequencing. Recent advancements in TGS technologies have significantly improved accuracy, a crucial requirement for the transition from research to diagnostic applications. Summary: In the field of immunohematology, the adoption of TGS is still in its early stages and published applications are scarce. An undeniable utility of TGS in blood group genomics is the ability to resolve ambiguous genotype-phenotype blood group results. In particular, hybrid genes and other large structural variants, as commonly found in the RHD/CE and MNS blood group systems, cause such discrepant results that can hardly be resolved by conventional methods. Long- read sequencing also greatly aids to generate high-standard reference alleles, establish haplotype sequence databases, or could even serve for high-resolution genotyping of all blood groups in parallel. Additionally, TGS holds the potential to close important knowledge gaps in blood group transcriptomics and epigenetics. Key Messages: The aims of this review were to examine the prospects of TGS technologies within the field of immunohematology and to highlight practical applications. Furthermore, we present a comprehensive overview of the existing and emerging wet-laboratory strategies for data generation, as well as a summary on bioinformatic data analysis methods. Finally, we provide an outlook on anticipated advancements in the near future. (c) 2023 The Author(s). Published by S. Karger AG, Basel
引用
收藏
页码:184 / 197
页数:14
相关论文
共 98 条
[1]   Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits [J].
Beyter, Doruk ;
Ingimundardottir, Helga ;
Oddsson, Asmundur ;
Eggertsson, Hannes P. ;
Bjornsson, Eythor ;
Jonsson, Hakon ;
Atlason, Bjarni A. ;
Kristmundsdottir, Snaedis ;
Mehringer, Svenja ;
Hardarson, Marteinn T. ;
Gudjonsson, Sigurjon A. ;
Magnusdottir, Droplaug N. ;
Jonasdottir, Aslaug ;
Jonasdottir, Adalbjorg ;
Kristjansson, Ragnar P. ;
Sverrisson, Sverrir T. ;
Holley, Guillaume ;
Palsson, Gunnar ;
Stefansson, Olafur A. ;
Eyjolfsson, Gudmundur ;
Olafsson, Isleifur ;
Sigurdardottir, Olof ;
Torfason, Bjarni ;
Masson, Gisli ;
Helgason, Agnar ;
Thorsteinsdottir, Unnur ;
Holm, Hilma ;
Gudbjartsson, Daniel F. ;
Sulem, Patrick ;
Magnusson, Olafur T. ;
Halldorsson, Bjarni, V ;
Stefansson, Kari .
NATURE GENETICS, 2021, 53 (06) :779-+
[2]   Rapid Characterization of Complex Killer Cell Immunoglobulin-Like Receptor (KIR) Regions Using Cas9 Enrichment and Nanopore Sequencing [J].
Bruijnesteijn, Jesse ;
van der Wiel, Marit ;
de Groot, Natasja G. ;
Bontrop, Ronald E. .
FRONTIERS IN IMMUNOLOGY, 2021, 12
[3]   Pacific biosciences sequencing technology for genotyping and variation discovery in human data [J].
Carneiro, Mauricio O. ;
Russ, Carsten ;
Ross, Michael G. ;
Gabriel, Stacey B. ;
Nusbaum, Chad ;
DePristo, Mark A. .
BMC GENOMICS, 2012, 13
[4]   Evolution of the human RH (rhesus) blood group genes: A 50 year old prediction (partially) fulfilled [J].
Carritt, B ;
Kemp, TJ ;
Poulter, M .
HUMAN MOLECULAR GENETICS, 1997, 6 (06) :843-850
[5]   Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia [J].
Chou, Stella T. ;
Flanagan, Jonathan M. ;
Vege, Sunitha ;
Luban, Naomi L. C. ;
Brown, R. Clark ;
Ware, Russell E. ;
Westhoff, Connie M. .
BLOOD ADVANCES, 2017, 1 (18) :1414-1422
[6]   DNA methylation: Bisulphite modification and analysis [J].
Clark, Susan J. ;
Statham, Aaron ;
Stirzaker, Clare ;
Molloy, Peter L. ;
Frommer, Marianne .
NATURE PROTOCOLS, 2006, 1 (05) :2353-2364
[7]   Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes [J].
Cohen, Ana S. A. ;
Farrow, Emily G. ;
Abdelmoity, Ahmed T. ;
Alaimo, Joseph T. ;
Amudhavalli, Shivarajan M. ;
Anderson, John T. ;
Bansal, Lalit ;
Bartik, Lauren ;
Baybayan, Primo ;
Belden, Bradley ;
Berrios, Courtney D. ;
Biswell, Rebecca L. ;
Buczkowicz, Pawel ;
Buske, Orion ;
Chakraborty, Shreyasee ;
Cheung, Warren A. ;
Coffman, Keith A. ;
Cooper, Ashley M. ;
Cross, Laura A. ;
Curran, Tom ;
Dang, Thuy Tien T. ;
Elfrink, Mary M. ;
Engleman, Kendra L. ;
Fecske, Erin D. ;
Fieser, Cynthia ;
Fitzgerald, Keely ;
Fleming, Emily A. ;
Gadea, Randi N. ;
Gannon, Jennifer L. ;
Gelineau-Morel, Rose N. ;
Gibson, Margaret ;
Goldstein, Jeffrey ;
Grundberg, Elin ;
Halpin, Kelsee ;
Harvey, Brian S. ;
Heese, Bryce A. ;
Hein, Wendy ;
Herd, Suzanne M. ;
Hughes, Susan S. ;
Ilyas, Mohammed ;
Jacobson, Jill ;
Jenkins, Janda L. ;
Jiang, Shao ;
Johnston, Jeffrey J. ;
Keeler, Kathryn ;
Korlach, Jonas ;
Kussmann, Jennifer ;
Lambert, Christine ;
Lawson, Caitlin ;
Le Pichon, Jean-Baptiste .
GENETICS IN MEDICINE, 2022, 24 (06) :1336-1348
[8]   A structural variation reference for medical and population genetics [J].
Collins, Ryan L. ;
Brand, Harrison ;
Karczewski, Konrad J. ;
Zhao, Xuefang ;
Alfoldi, Jessica ;
Francioli, Laurent C. ;
Khera, Amit, V ;
Lowther, Chelsea ;
Gauthier, Laura D. ;
Wang, Harold ;
Watts, Nicholas A. ;
Solomonson, Matthew ;
O'Donnell-Luria, Anne ;
Baumann, Alexander ;
Munshi, Ruchi ;
Walker, Mark ;
Whelan, Christopher W. ;
Huang, Yongqing ;
Brookings, Ted ;
Sharpe, Ted ;
Stone, Matthew R. ;
Valkanas, Elise ;
Fu, Jack ;
Tiao, Grace ;
Laricchia, Kristen M. ;
Ruano-Rubio, Valentin ;
Stevens, Christine ;
Gupta, Namrata ;
Cusick, Caroline ;
Margolin, Lauren ;
Taylor, Kent D. ;
Lin, Henry J. ;
Rich, Stephen S. ;
Post, Wendy S. ;
Chen, Yii-Der Ida ;
Rotter, Jerome, I ;
Nusbaum, Chad ;
Philippakis, Anthony ;
Lander, Eric ;
Gabriel, Stacey ;
Neale, Benjamin M. ;
Kathiresan, Sekar ;
Daly, Mark J. ;
Banks, Eric ;
MacArthur, Daniel G. ;
Talkowski, Michael E. .
NATURE, 2020, 581 (7809) :444-+
[9]   Missense mutations in PIEZO1, which encodes the Piezo1 mechanosensor protein, define Er red blood cell antigens [J].
Crew, Vanja Karamatic ;
Tilley, Louise A. ;
Satchwell, Timothy J. ;
AlSubhi, Samah A. ;
Jones, Benjamin ;
Spring, Frances A. ;
Walser, Piers J. ;
Freire, Catarina Martins ;
Murciano, Nicoletta ;
Rotordam, Maria Giustina ;
Woestmann, Svenja J. ;
Hamed, Marwa ;
Alradwan, Reem ;
AlKhrousey, Mouza ;
Skidmore, Ian ;
Lewis, Sarah ;
Hussain, Shimon ;
Jackson, Jane ;
Latham, Tom ;
Kiloy, Mark D. ;
Lester, William ;
Becker, Nadine ;
Rapedius, Markus ;
Toye, Ashley M. ;
Thornton, Nicole M. .
BLOOD, 2023, 141 (02) :135-146
[10]  
Daniels G, 2013, Human Blood Groups, V3rd