Personal genomics (English Wikipedia)

"Privacy and Progress in Whole Genome Sequencing". Presidential Commission for the Study of Bioethical Issues. Archived from the original on 22 November 2016. Retrieved 30 November 2016.

bloomberg.com

Lauerman, John (5 February 2009). "Complete Genomics Drives Down Cost of Genome Sequence to $5,000". Bloomberg. Retrieved 19 October 2011.

cancer.gov

"NCI Dictionary of Cancer Terms". National Cancer Institute. 2 February 2011. Retrieved 5 December 2016.

claudiacopeland.com

Copeland, CS (May–June 2014). "What a Tangled Web We Weave" (PDF). Healthcare Journal of Little Rock.
Copeland, CS (March–April 2014). "Individual Freedom, Public Safety, and the Complex Frontier of Personal Genomics" (PDF). Healthcare Journal of New Orleans.

cleveland.com

Caniglia, John (21 June 2018). "Authorities solve cold case of war hero who hid behind dead boy's identity". cleveland.com. Retrieved 22 June 2018.

doi.org

Strausberg, Robert L.; Simpson, Andrew J. G.; Old, Lloyd J.; Riggins, Gregory J. (27 May 2004). "Oncogenomics and the development of new cancer therapies". Nature. 429 (6990): 469–474. Bibcode:2004Natur.429..469S. doi:10.1038/nature02627. PMID 15164073. S2CID 37628107.
Johnson, Julie A (5 December 2016). "Pharmacogenetics in clinical practice: how far have we come and where are we going?". Pharmacogenomics. 14 (7): 835–843. doi:10.2217/pgs.13.52. PMC 3697735. PMID 23651030.
Wheeler, David A; Srinivasan, Maithreyan; Egholm, Michael; Shen, Yufeng; Chen, Lei; McGuire, Amy; He, Wen; Chen, Yi-Ju; Makhijani, Vinod; Roth, G. Thomas; Gomes, Xavier; Tartaro, Karrie; Niazi, Faheem; Turcotte, Cynthia L; Irzyk, Gerard P; Lupski, James R; Chinault, Craig; Song, Xing-zhi; Liu, Yue; Yuan, Ye; Nazareth, Lynne; Qin, Xiang; Muzny, Donna M; Margulies, Marcel; Weinstock, George M; Gibbs, Richard A; Rothberg, Jonathan M (2008). "JDW-genome-supp-mat-march-proof.doc" (PDF). Nature. 452 (7189): 872–876. Bibcode:2008Natur.452..872W. doi:10.1038/nature06884. PMID 18421352. S2CID 4429736. Retrieved 19 October 2011.
Greshake, Bastian (2014). "openSNP–A Crowdsourced Web Resource for Personal Genomics". PLOS ONE. 9 (3): e89204. Bibcode:2014PLoSO...989204G. doi:10.1371/journal.pone.0089204. PMC 3960092. PMID 24647222.
Corpas, Manuel (2013). "Crowdsourcing the Corpasome". Source Code for Biology and Medicine. 8 (1): 13. doi:10.1186/1751-0473-8-13. PMC 3706263. PMID 23799911.
Corpas M, Valdivia-Granda W, Torres N, Greshake B, Coletta A, Knaus A, Harrison AP, Cariaso M, Moran F, Nielsen F, Swan D, Weiss Solis DY, Krawitz P, Schacherer F, Schols P, Yang H, Borry P, Glusman G, Robinson PN (November 2015). "Crowdsourced direct-to-consumer genomic analysis of a family quartet". BMC Genomics. 16 (910): 910. doi:10.1186/s12864-015-1973-7. PMC 4636840. PMID 26547235.
McCabe LL; McCabe ER (June 2001). "Postgenomic medicine. Presymptomatic testing for prediction and prevention". Clin Perinatol. 28 (2): 425–34. doi:10.1016/S0095-5108(05)70094-4. PMID 11499063.
Nelson RM; Botkjin JR; Kodish ED; et al. (June 2001). "Ethical issues with genetic testing in pediatrics". Pediatrics. 107 (6): 1451–55. doi:10.1542/peds.107.6.1451. PMID 11389275.
Borry P; Fryns JP; Schotsmans P; Dierickx K (February 2006). "Carrier testing in minors: a systematic review of guidelines and position papers". Eur. J. Hum. Genet. 14 (2): 133–8. doi:10.1038/sj.ejhg.5201509. PMID 16267502.
Borry P; Stultiens L; Nys H; Cassiman JJ; et al. (November 2006). "Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers". Clin. Genet. 70 (5): 374–81. doi:10.1111/j.1399-0004.2006.00692.x. PMID 17026616. S2CID 7066285.
de Vries, Jantina; Bull, Susan J; Doumbo, Ogobara; Ibrahim, Muntaser; Mercereau-Puijalon, Odile; Kwiatkowski, Dominic; Parker, Michael (18 March 2011). "Ethical issues in human genomics research in developing countries". BMC Medical Ethics. 12: 5. doi:10.1186/1472-6939-12-5. PMC 3076260. PMID 21418562.
Check Hayden, Erika (2013). "Privacy loophole found in genetic databases". Nature. doi:10.1038/nature.2013.12237. S2CID 211729032.
Gutmann, Amy; Wagner, James W. (1 May 2013). "Found Your DNA on the Web: Reconciling Privacy and Progress". Hastings Center Report. 43 (3): 15–18. doi:10.1002/hast.162. PMID 23650063.
Mao Q, Ciotlos S, Zhang RY, Ball MP, Chin R, Carnevali P, Barua N, Nguyen S, Agarwal MR, Clegg T, Connelly A, Vandewege W, Zaranek AW, Estep PW, Church GM, Drmanac R, Peters BA (2016). "The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes". GigaScience. 5 (1): 42. doi:10.1186/s13742-016-0148-z. PMC 5057367. PMID 27724973.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Cai B, Li B, Kiga N, Thusberg J, Bergquist T, Chen Y, Niknafs N, Carter H, Tokheim C, Beleva-Guthrie V, Douville C, Bhattacharya R, Yeo HTG, Fan J, Sengupta S, Kim D, Cline M, Turner T, Diekhans M, Zaucha J, Pal L, Cao C, Yu C, Yin Y, Carraro M, Giollo M, Ferrari C, Leonardi E, Tosatto SCE, Bobe J, Ball M, Hoskins R, Repo S, Church G, Brenner S, Moult J, Gough J, Stanke M, Karchin R, Mooney SD (2016). "Matching Phenotypes to Whole Genomes: Lessons Learned from Three Iterations of the Personal Genome Project Community Challenges". Human Mutation. 38 (9): 1266–1276. doi:10.1002/humu.23265. PMC 5645203. PMID 28544481.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Check Hayden, Erika (2016). "Rethink the links between genes and disease: The ExAC database has shown that many mutations thought to be harmful are benign". Nature. 538 (7624): 140. doi:10.1038/538140a. PMID 27734882.
Hunter, David J.; Khoury, Muin J.; Drazen, Jeffrey M. (10 January 2008). "Letting the Genome out of the Bottle – Will We Get Our Wish?". New England Journal of Medicine. 358 (2): 105–107. doi:10.1056/NEJMp0708162. PMID 18184955.
Corpas, Manuel (6 January 2012). "A Family Experience of Personal Genomics". Journal of Genetic Counseling. 21 (3): 368–391. doi:10.1007/s10897-011-9473-7. PMID 22223063. S2CID 10845045.

everygenome.com

"Individual genome sequencing – Illumina, Inc". Everygenome.com. Archived from the original on 19 October 2011. Retrieved 19 October 2011.

fda.gov

Research, Center for Drug Evaluation and. "Genomics - Table of Pharmacogenomic Biomarkers in Drug Labeling". www.fda.gov. Archived from the original on 14 June 2009. Retrieved 5 December 2016.

forensicmag.com

"'Buck Skin Girl' Case Break Is Success of New DNA Doe Project". Forensic Magazine. 16 April 2018. Retrieved 22 June 2018.
"DNA Doe Project IDs 2001 Motel Suicide, Using Genealogy". Forensic Magazine. 9 May 2018. Retrieved 22 June 2018.

future-science-group.com

Lunshof, Jeantine; Mardis Elaine [Retrieved from http://www.future-science-group.com/_img/pics/Mardis_Forward.pdf^{[permanent dead link]} "Navigenics - How it works"]. Future Medicine Magazine. Retrieved 30 March 2012/

genome.gov

Wetterstrand, Kris (21 May 2012). "DNA Sequencing Costs: Data from the NHGRI Large-Scale Genome Sequencing Program". Large-Scale Genome Sequencing Program. National Human Genome Research Institute. Retrieved 24 May 2012.
"The Cost of Sequencing a Human Genome". National Human Genome Research Institute (NHGRI). Retrieved 5 December 2016.
"Genetic Discrimination". National Human Genome Research Institute (NHGRI). Retrieved 5 December 2016.

genomes2people.org

Roberts, J. Scott; Gornick, Michele C. et al [Retrieved from http://www.genomes2people.org/wp-content/uploads/2017/01/Roberts-et-al-PGen-PHG-2017.pdf "Direct-to-Consumer Genetic Testing: User Motivations, Decision Making, and Perceived Utility of Results"]. Public Health Genomics. Retrieved 20 February 2017/

genomeweb.com

Karow, Julia (19 May 2009). "Knome Adds Exome Sequencing, Starts Offering Services to Researchers". GenomeWeb. Retrieved 24 February 2010.
Karow, Julia (4 November 2008). "Complete Genomics to Offer $5,000 Human Genome as a Service Business in Q2 2009 | In Sequence | Sequencing". GenomeWeb. Retrieved 19 October 2011.
"ACMG Updates Secondary Findings Gene List". GenomeWeb. 17 November 2016.

glgroup.com

"Illumina Cutting Personal Genome Sequencing Price by 60% | GPlus.com". Glgroup.com. 4 June 2010. Retrieved 19 October 2011.

harvard.edu

ui.adsabs.harvard.edu

Strausberg, Robert L.; Simpson, Andrew J. G.; Old, Lloyd J.; Riggins, Gregory J. (27 May 2004). "Oncogenomics and the development of new cancer therapies". Nature. 429 (6990): 469–474. Bibcode:2004Natur.429..469S. doi:10.1038/nature02627. PMID 15164073. S2CID 37628107.
Wheeler, David A; Srinivasan, Maithreyan; Egholm, Michael; Shen, Yufeng; Chen, Lei; McGuire, Amy; He, Wen; Chen, Yi-Ju; Makhijani, Vinod; Roth, G. Thomas; Gomes, Xavier; Tartaro, Karrie; Niazi, Faheem; Turcotte, Cynthia L; Irzyk, Gerard P; Lupski, James R; Chinault, Craig; Song, Xing-zhi; Liu, Yue; Yuan, Ye; Nazareth, Lynne; Qin, Xiang; Muzny, Donna M; Margulies, Marcel; Weinstock, George M; Gibbs, Richard A; Rothberg, Jonathan M (2008). "JDW-genome-supp-mat-march-proof.doc" (PDF). Nature. 452 (7189): 872–876. Bibcode:2008Natur.452..872W. doi:10.1038/nature06884. PMID 18421352. S2CID 4429736. Retrieved 19 October 2011.
Greshake, Bastian (2014). "openSNP–A Crowdsourced Web Resource for Personal Genomics". PLOS ONE. 9 (3): e89204. Bibcode:2014PLoSO...989204G. doi:10.1371/journal.pone.0089204. PMC 3960092. PMID 24647222.

healthcarejournallr.com

http://www.healthcarejournallr.com/the-journal/contents-index/features/563-what-a-tangled-web-we-weave.html}^{[permanent dead link]}

helicosbio.com

"True Single Molecule Sequencing (tSMS): Helicos BioSciences". Helicosbio.com. Archived from the original on 4 October 2011. Retrieved 19 October 2011.

jsonline.com

Mark Johnson & Kathleen Gallagher (27 February 2011). "One in a Billion. Nic Volker case may be the leading edge of a wave moving across genetic medicine". Milwaukee Journal Sentinel.

kuleuven.be

lirias.kuleuven.be

Borry P; Stultiens L; Nys H; Cassiman JJ; et al. (November 2006). "Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers". Clin. Genet. 70 (5): 374–81. doi:10.1111/j.1399-0004.2006.00692.x. PMID 17026616. S2CID 7066285.

medium.com

genomes2people.medium.com

"Is Preventive Genomics Elitist?". 21 October 2019.

mrc.ac.uk

MRC, Medical Research Council (3 March 2016). "Stratified medicine". www.mrc.ac.uk. Retrieved 5 December 2016.

msn.com

news.moneycentral.msn.com

"MSN | Outlook, Office, Skype, Bing, Breaking News, and Latest Videos". Archived from the original on 25 August 2009. Retrieved 11 June 2009.

nature.com

"Predictive medicine - Latest research and news | Nature". www.nature.com. Retrieved 5 December 2016.
Wheeler, David A; Srinivasan, Maithreyan; Egholm, Michael; Shen, Yufeng; Chen, Lei; McGuire, Amy; He, Wen; Chen, Yi-Ju; Makhijani, Vinod; Roth, G. Thomas; Gomes, Xavier; Tartaro, Karrie; Niazi, Faheem; Turcotte, Cynthia L; Irzyk, Gerard P; Lupski, James R; Chinault, Craig; Song, Xing-zhi; Liu, Yue; Yuan, Ye; Nazareth, Lynne; Qin, Xiang; Muzny, Donna M; Margulies, Marcel; Weinstock, George M; Gibbs, Richard A; Rothberg, Jonathan M (2008). "JDW-genome-supp-mat-march-proof.doc" (PDF). Nature. 452 (7189): 872–876. Bibcode:2008Natur.452..872W. doi:10.1038/nature06884. PMID 18421352. S2CID 4429736. Retrieved 19 October 2011.
Check Hayden, Erika (2013). "Privacy loophole found in genetic databases". Nature. doi:10.1038/nature.2013.12237. S2CID 211729032.

ncsl.org

"Genetics and Health Insurance State Anti-Discrimination Laws".

nih.gov

pubmed.ncbi.nlm.nih.gov

Strausberg, Robert L.; Simpson, Andrew J. G.; Old, Lloyd J.; Riggins, Gregory J. (27 May 2004). "Oncogenomics and the development of new cancer therapies". Nature. 429 (6990): 469–474. Bibcode:2004Natur.429..469S. doi:10.1038/nature02627. PMID 15164073. S2CID 37628107.
Johnson, Julie A (5 December 2016). "Pharmacogenetics in clinical practice: how far have we come and where are we going?". Pharmacogenomics. 14 (7): 835–843. doi:10.2217/pgs.13.52. PMC 3697735. PMID 23651030.
Wheeler, David A; Srinivasan, Maithreyan; Egholm, Michael; Shen, Yufeng; Chen, Lei; McGuire, Amy; He, Wen; Chen, Yi-Ju; Makhijani, Vinod; Roth, G. Thomas; Gomes, Xavier; Tartaro, Karrie; Niazi, Faheem; Turcotte, Cynthia L; Irzyk, Gerard P; Lupski, James R; Chinault, Craig; Song, Xing-zhi; Liu, Yue; Yuan, Ye; Nazareth, Lynne; Qin, Xiang; Muzny, Donna M; Margulies, Marcel; Weinstock, George M; Gibbs, Richard A; Rothberg, Jonathan M (2008). "JDW-genome-supp-mat-march-proof.doc" (PDF). Nature. 452 (7189): 872–876. Bibcode:2008Natur.452..872W. doi:10.1038/nature06884. PMID 18421352. S2CID 4429736. Retrieved 19 October 2011.
Greshake, Bastian (2014). "openSNP–A Crowdsourced Web Resource for Personal Genomics". PLOS ONE. 9 (3): e89204. Bibcode:2014PLoSO...989204G. doi:10.1371/journal.pone.0089204. PMC 3960092. PMID 24647222.
Corpas, Manuel (2013). "Crowdsourcing the Corpasome". Source Code for Biology and Medicine. 8 (1): 13. doi:10.1186/1751-0473-8-13. PMC 3706263. PMID 23799911.
Corpas M, Valdivia-Granda W, Torres N, Greshake B, Coletta A, Knaus A, Harrison AP, Cariaso M, Moran F, Nielsen F, Swan D, Weiss Solis DY, Krawitz P, Schacherer F, Schols P, Yang H, Borry P, Glusman G, Robinson PN (November 2015). "Crowdsourced direct-to-consumer genomic analysis of a family quartet". BMC Genomics. 16 (910): 910. doi:10.1186/s12864-015-1973-7. PMC 4636840. PMID 26547235.
McCabe LL; McCabe ER (June 2001). "Postgenomic medicine. Presymptomatic testing for prediction and prevention". Clin Perinatol. 28 (2): 425–34. doi:10.1016/S0095-5108(05)70094-4. PMID 11499063.
Nelson RM; Botkjin JR; Kodish ED; et al. (June 2001). "Ethical issues with genetic testing in pediatrics". Pediatrics. 107 (6): 1451–55. doi:10.1542/peds.107.6.1451. PMID 11389275.
Borry P; Fryns JP; Schotsmans P; Dierickx K (February 2006). "Carrier testing in minors: a systematic review of guidelines and position papers". Eur. J. Hum. Genet. 14 (2): 133–8. doi:10.1038/sj.ejhg.5201509. PMID 16267502.
Borry P; Stultiens L; Nys H; Cassiman JJ; et al. (November 2006). "Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers". Clin. Genet. 70 (5): 374–81. doi:10.1111/j.1399-0004.2006.00692.x. PMID 17026616. S2CID 7066285.
de Vries, Jantina; Bull, Susan J; Doumbo, Ogobara; Ibrahim, Muntaser; Mercereau-Puijalon, Odile; Kwiatkowski, Dominic; Parker, Michael (18 March 2011). "Ethical issues in human genomics research in developing countries". BMC Medical Ethics. 12: 5. doi:10.1186/1472-6939-12-5. PMC 3076260. PMID 21418562.
Gutmann, Amy; Wagner, James W. (1 May 2013). "Found Your DNA on the Web: Reconciling Privacy and Progress". Hastings Center Report. 43 (3): 15–18. doi:10.1002/hast.162. PMID 23650063.
Mao Q, Ciotlos S, Zhang RY, Ball MP, Chin R, Carnevali P, Barua N, Nguyen S, Agarwal MR, Clegg T, Connelly A, Vandewege W, Zaranek AW, Estep PW, Church GM, Drmanac R, Peters BA (2016). "The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes". GigaScience. 5 (1): 42. doi:10.1186/s13742-016-0148-z. PMC 5057367. PMID 27724973.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Cai B, Li B, Kiga N, Thusberg J, Bergquist T, Chen Y, Niknafs N, Carter H, Tokheim C, Beleva-Guthrie V, Douville C, Bhattacharya R, Yeo HTG, Fan J, Sengupta S, Kim D, Cline M, Turner T, Diekhans M, Zaucha J, Pal L, Cao C, Yu C, Yin Y, Carraro M, Giollo M, Ferrari C, Leonardi E, Tosatto SCE, Bobe J, Ball M, Hoskins R, Repo S, Church G, Brenner S, Moult J, Gough J, Stanke M, Karchin R, Mooney SD (2016). "Matching Phenotypes to Whole Genomes: Lessons Learned from Three Iterations of the Personal Genome Project Community Challenges". Human Mutation. 38 (9): 1266–1276. doi:10.1002/humu.23265. PMC 5645203. PMID 28544481.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Machácková, E. (1 March 2003). "Disease-causing mutations versus neutral polymorphism: use of bioinformatics and DNA diagnosis". Casopis Lekaru Ceskych. 142 (3): 150–153. PMID 12756842.
Check Hayden, Erika (2016). "Rethink the links between genes and disease: The ExAC database has shown that many mutations thought to be harmful are benign". Nature. 538 (7624): 140. doi:10.1038/538140a. PMID 27734882.
Hunter, David J.; Khoury, Muin J.; Drazen, Jeffrey M. (10 January 2008). "Letting the Genome out of the Bottle – Will We Get Our Wish?". New England Journal of Medicine. 358 (2): 105–107. doi:10.1056/NEJMp0708162. PMID 18184955.
Corpas, Manuel (6 January 2012). "A Family Experience of Personal Genomics". Journal of Genetic Counseling. 21 (3): 368–391. doi:10.1007/s10897-011-9473-7. PMID 22223063. S2CID 10845045.

ncbi.nlm.nih.gov

Johnson, Julie A (5 December 2016). "Pharmacogenetics in clinical practice: how far have we come and where are we going?". Pharmacogenomics. 14 (7): 835–843. doi:10.2217/pgs.13.52. PMC 3697735. PMID 23651030.
"Gene Tests".
Greshake, Bastian (2014). "openSNP–A Crowdsourced Web Resource for Personal Genomics". PLOS ONE. 9 (3): e89204. Bibcode:2014PLoSO...989204G. doi:10.1371/journal.pone.0089204. PMC 3960092. PMID 24647222.
Corpas, Manuel (2013). "Crowdsourcing the Corpasome". Source Code for Biology and Medicine. 8 (1): 13. doi:10.1186/1751-0473-8-13. PMC 3706263. PMID 23799911.
Corpas M, Valdivia-Granda W, Torres N, Greshake B, Coletta A, Knaus A, Harrison AP, Cariaso M, Moran F, Nielsen F, Swan D, Weiss Solis DY, Krawitz P, Schacherer F, Schols P, Yang H, Borry P, Glusman G, Robinson PN (November 2015). "Crowdsourced direct-to-consumer genomic analysis of a family quartet". BMC Genomics. 16 (910): 910. doi:10.1186/s12864-015-1973-7. PMC 4636840. PMID 26547235.
de Vries, Jantina; Bull, Susan J; Doumbo, Ogobara; Ibrahim, Muntaser; Mercereau-Puijalon, Odile; Kwiatkowski, Dominic; Parker, Michael (18 March 2011). "Ethical issues in human genomics research in developing countries". BMC Medical Ethics. 12: 5. doi:10.1186/1472-6939-12-5. PMC 3076260. PMID 21418562.
Mao Q, Ciotlos S, Zhang RY, Ball MP, Chin R, Carnevali P, Barua N, Nguyen S, Agarwal MR, Clegg T, Connelly A, Vandewege W, Zaranek AW, Estep PW, Church GM, Drmanac R, Peters BA (2016). "The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes". GigaScience. 5 (1): 42. doi:10.1186/s13742-016-0148-z. PMC 5057367. PMID 27724973.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Cai B, Li B, Kiga N, Thusberg J, Bergquist T, Chen Y, Niknafs N, Carter H, Tokheim C, Beleva-Guthrie V, Douville C, Bhattacharya R, Yeo HTG, Fan J, Sengupta S, Kim D, Cline M, Turner T, Diekhans M, Zaucha J, Pal L, Cao C, Yu C, Yin Y, Carraro M, Giollo M, Ferrari C, Leonardi E, Tosatto SCE, Bobe J, Ball M, Hoskins R, Repo S, Church G, Brenner S, Moult J, Gough J, Stanke M, Karchin R, Mooney SD (2016). "Matching Phenotypes to Whole Genomes: Lessons Learned from Three Iterations of the Personal Genome Project Community Challenges". Human Mutation. 38 (9): 1266–1276. doi:10.1002/humu.23265. PMC 5645203. PMID 28544481.{{cite journal}}: CS1 maint: multiple names: authors list (link)

ghr.nlm.nih.gov

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rarediseases.info.nih.gov

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nytimes.com

Arango, Tim; Goldman, Adam; Fuller, Thomas (27 April 2018). "To Catch a Killer: A Fake Profile on a DNA Site and a Pristine Sample". The New York Times.
Haag, Matthew (4 February 2019). "FamilyTreeDNA Admits to Sharing Genetic Data With F.B.I." The New York Times. ISSN 0362-4331. Retrieved 11 February 2019.

scienceblogs.com

"Illumina launches personal genome sequencing service for $48,000 : Genetic Future". Scienceblogs.com. Archived from the original on 6 June 2011. Retrieved 19 October 2011.

scientificamerican.com

Harmon, Katherine (28 June 2010). "Genome Sequencing for the Rest of Us". Scientific American. Retrieved 13 August 2010.

semanticscholar.org

api.semanticscholar.org

Strausberg, Robert L.; Simpson, Andrew J. G.; Old, Lloyd J.; Riggins, Gregory J. (27 May 2004). "Oncogenomics and the development of new cancer therapies". Nature. 429 (6990): 469–474. Bibcode:2004Natur.429..469S. doi:10.1038/nature02627. PMID 15164073. S2CID 37628107.
Wheeler, David A; Srinivasan, Maithreyan; Egholm, Michael; Shen, Yufeng; Chen, Lei; McGuire, Amy; He, Wen; Chen, Yi-Ju; Makhijani, Vinod; Roth, G. Thomas; Gomes, Xavier; Tartaro, Karrie; Niazi, Faheem; Turcotte, Cynthia L; Irzyk, Gerard P; Lupski, James R; Chinault, Craig; Song, Xing-zhi; Liu, Yue; Yuan, Ye; Nazareth, Lynne; Qin, Xiang; Muzny, Donna M; Margulies, Marcel; Weinstock, George M; Gibbs, Richard A; Rothberg, Jonathan M (2008). "JDW-genome-supp-mat-march-proof.doc" (PDF). Nature. 452 (7189): 872–876. Bibcode:2008Natur.452..872W. doi:10.1038/nature06884. PMID 18421352. S2CID 4429736. Retrieved 19 October 2011.
Borry P; Stultiens L; Nys H; Cassiman JJ; et al. (November 2006). "Presymptomatic and predictive genetic testing in minors: a systematic review of guidelines and position papers". Clin. Genet. 70 (5): 374–81. doi:10.1111/j.1399-0004.2006.00692.x. PMID 17026616. S2CID 7066285.
Check Hayden, Erika (2013). "Privacy loophole found in genetic databases". Nature. doi:10.1038/nature.2013.12237. S2CID 211729032.
Corpas, Manuel (6 January 2012). "A Family Experience of Personal Genomics". Journal of Genetic Counseling. 21 (3): 368–391. doi:10.1007/s10897-011-9473-7. PMID 22223063. S2CID 10845045.

slate.com

Bala, Nila (18 March 2019). "Criminal Suspects Deserve Genetic Privacy, Too". Slate Magazine.

statnews.com

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theatlantic.com

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thegeneticgenealogist.com

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vancouversun.com

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washingtonpost.com

Kaplan, Sarah (17 April 2016). "How do your 20,000 genes determine so many wildly different traits? They multitask". The Washington Post. Retrieved 27 August 2016.

web.archive.org

Research, Center for Drug Evaluation and. "Genomics - Table of Pharmacogenomic Biomarkers in Drug Labeling". www.fda.gov. Archived from the original on 14 June 2009. Retrieved 5 December 2016.
"True Single Molecule Sequencing (tSMS): Helicos BioSciences". Helicosbio.com. Archived from the original on 4 October 2011. Retrieved 19 October 2011.
"Individual genome sequencing – Illumina, Inc". Everygenome.com. Archived from the original on 19 October 2011. Retrieved 19 October 2011.
"MSN | Outlook, Office, Skype, Bing, Breaking News, and Latest Videos". Archived from the original on 25 August 2009. Retrieved 11 June 2009.
"Illumina launches personal genome sequencing service for $48,000 : Genetic Future". Scienceblogs.com. Archived from the original on 6 June 2011. Retrieved 19 October 2011.
"Privacy and Progress in Whole Genome Sequencing". Presidential Commission for the Study of Bioethical Issues. Archived from the original on 22 November 2016. Retrieved 30 November 2016.

wired.com

Megan Molteni (19 November 2018). "Now You Can Sequence Your Whole Genome For Just $200". Wired.

worldcat.org

search.worldcat.org

Haag, Matthew (4 February 2019). "FamilyTreeDNA Admits to Sharing Genetic Data With F.B.I." The New York Times. ISSN 0362-4331. Retrieved 11 February 2019.