 Whole Genome Sequencing
"Whole Genome Sequencing" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Techniques to determine the entire sequence of the GENOME of an organism or individual.
| Descriptor ID |
D000073336
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| MeSH Number(s) |
E05.393.760.700.825
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| Concept/Terms |
Whole Genome Sequencing- Whole Genome Sequencing
- Genome Sequencing, Whole
- Sequencing, Whole Genome
- Complete Genome Sequencing
- Genome Sequencing, Complete
- Sequencing, Complete Genome
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Below are MeSH descriptors whose meaning is more general than "Whole Genome Sequencing".
Below are MeSH descriptors whose meaning is more specific than "Whole Genome Sequencing".
This graph shows the total number of publications written about "Whole Genome Sequencing" by people in this website by year, and whether "Whole Genome Sequencing" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 2 | 3 | | 2016 | 0 | 1 | 1 | | 2017 | 3 | 4 | 7 | | 2018 | 2 | 9 | 11 | | 2019 | 4 | 7 | 11 | | 2020 | 5 | 8 | 13 | | 2021 | 7 | 20 | 27 | | 2022 | 1 | 9 | 10 | | 2023 | 2 | 4 | 6 | | 2024 | 6 | 7 | 13 | | 2025 | 8 | 13 | 21 | | 2026 | 3 | 4 | 7 |
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Below are the most recent publications written about "Whole Genome Sequencing" by people in Profiles.
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Chiles JW, Rocco A, Srinivasasainagendra V, Rossiter HB, Casaburi R, Thalacker-Mercer A, Wells JM, Wan ES, Silverman EK, Cho MH, Hersh CP, Psaty BM, Gharib SA, Gao Y, O'Connor GT, Lange LA, Rich SS, Manichaikul AW, Barr RG, Ortega VE, Meyers DA, Smith AV, Tiwari HK, McDonald MN. Whole Genome Sequence Analysis of Weight Loss in 16?972 Participants With COPD Reveals Novel Risk Loci in DRAIC and RFX3. J Cachexia Sarcopenia Muscle. 2026 Jun; 17(3):e70293.
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Hansen A, Luca S, Moran O, Babul-Hirji R, Coe TB, Wilk K, Assamad D, Fooks K, Venkataramanan V, Shickh S, Yan J, Wu V, Badalato L, Balci TB, Ladouceur VB, Chad L, Chisholm C, Gillespie MK, Huang L, Jarinova O, Lau L, Lee W, Mackley MP, Marshall CR, Mendoza-Londono R, Morel CF, Richer J, Sawyer S, Stavropoulos DJ, Szuto A, Tarnopolsky M, Villani A, Zahavich L, Somerville MJ, Boycott KM, Ungar WJ, Hayeems RZ. Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing. J Genet Couns. 2026 Jun; 35(3):e70218.
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Aquino YSJ, Scarfe J, Popic D, Carolan L, Degeling C, Prokopovich K, Otlowski MFA, Singh S, Fabrianesi B, Bhattacharya K, Jones K, Newson AJ, Shih P, Bennetts B, Frost E, Stark ZL, Nowak K, Healy L, Norris S, Carter SM. Genomic Newborn Screening: Verdict From an Australian Citizens' Jury. Med J Aust. 2026 04; 224(4):e70184.
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Ivancevic A, Sankovitz M, Allen H, Joyner O, Chuong EB, Ramsey SD. Whole-genome sequences of the dwarf honey bee subgenus Micrapis: Apis andreniformis and Apis florea. G3 (Bethesda). 2026 03 04; 16(3).
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Penaranda C, Brenner EP, Clatworthy AE, Cosimi LA, Ravi J, Hung DT. Genomic comparison and phenotypic characterization of Pseudomonas aeruginosa isolates across environmental and diverse clinical isolation sites. mSystems. 2026 Mar 24; 11(3):e0136225.
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Ramsay M, Etheredge H, Tluway F, D'Amato ME, Chikwambi Z, Hamdi Y, Alhudiri I, Fakim Y, Ahmad KM, Belguith N, Bentley D, Boujemaa M, Calumbuana N, Chaouch M, Charfeddine C, Chinien G, Dukuze N, Eljilani M, Elzagheid A, Ferraz N, Ghoorah A, Goorah S, Gribaa M, Guidara S, Guirat M, Hazelhurst S, Jallul M, Kasu M, Kharrat N, Khumalo U, Kingsbury Z, Kisiangani I, Lopes-Cendes I, Lukusa P, Makay P, Makulo J, Mubungu G, Muhinda C, Mukhongo DM, Murwira A, Mustafa A, Ndinkabandi J, Ngole M, Nlandu Y, Nyathi M, Pereira L, Rejeb I, Santos LL, Sengupta D, Shebani A, Smyth N, Souissi A, Trabelsi M, Rebai A, Chimpolo MM, Lumaka A, Masimirembwa C, Mohamed SF, Mulder N, Mutesa L, Hanchard NA, Choudhury A. Enriching African genome representation through the AGenDA project. Nature. 2026 01; 649(8097):565-573.
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Chu VT, Spottiswoode N, Ward R, Yokoe DS, Ramirez-Avila L, Phelps MS, Glascock A, Crawford ED, Kamm J, Hao S, Li L, Dynerman D, Waltari E, Nafees S, Kalantar KL, Caldera S, Madera S, Guerrero ES, Ivashin D, Serpa PH, Love C, Mwakibete LL, Doernberg SB, Kistler A, Alvino R, Engel J, Chiu CY, Pak C, Cunningham G, Reyes H, Buie B, Messacar K, Leroue M, Prince BC, Detweiler AM, Stanley K, Caughell C, McNeil N, Neff N, Nichols A, Miller S, DeRisi JL, Tato CM, Langelier CR. Implementation and outcomes of a rapid response genomic hospital epidemiology programme at an academic medical centre over 7 years. Lancet Microbe. 2026 Feb; 7(2):101277.
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Van Buren E, Zhang Y, Li X, Selvaraj MS, Li Z, Zhou H, Palmer ND, Arnett DK, Blangero J, Boerwinkle E, Cade BE, Carlson JC, Carson AP, Chen YI, Curran J, Duggirala R, Fornage M, Franceschini N, Graff M, Gu C, Guo X, He J, Heard-Cosa N, Hou L, Hung YJ, Kalyani RR, Kardia SLR, Kenny E, Kooperberg C, Kral BG, Lange L, Levy D, Li C, Liu S, Lloyd-Jones D, Loos RJF, Manichaikul AW, Martin LW, Mathias R, Minster RL, Mitchell BD, Mychaleckyj JC, Naseri T, North K, O'Connell J, Perry JA, Peyser PA, Psaty BM, Raffield LM, Vasan RS, Redline S, Reiner AP, Rich SS, Smith JA, Spitzer B, Tang H, Taylor KD, Tracy R, Viali S, Yanek L, Zhao W, Rotter JI, Peloso GM, Natarajan P, Lin X. cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions. Nat Methods. 2026 Feb; 23(2):338-349.
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Hunt DR, Allen H, Martin TG, Feghali SN, Chuong EB, Leinwand LA. Genome report: first whole genome assembly of Python regius (ball python), a model of extreme physiological and metabolic plasticity. G3 (Bethesda). 2025 11 12; 15(11).
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Sato T, Kubo D, Hirasawa Y, Yoneda M, Kimura R, Tajima A, Kato H. Genome of an early Okhotsk individual reveals ancient admixture between Jomon and Kamchatka lineages. Sci Rep. 2025 Oct 27; 15(1):37520.
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