Linked-read sequencing (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Linked-read sequencing" in English language version.

refsWebsite

Global rank English rank

28nih.gov

4^th place

14doi.org

2^nd place

14worldcat.org

5^th place

3harvard.edu

18^th place

17^th place

1oup.com

485^th place

440^th place

1justia.com

696^th place

428^th place

doi.org

Marks, Patrick; Garcia, Sarah; Barrio, Alvaro Martinez; Belhocine, Kamila; Bernate, Jorge; Bharadwaj, Rajiv; Bjornson, Keith; Catalanotti, Claudia; Delaney, Josh; Fehr, Adrian; Fiddes, Ian T.; Galvin, Brendan; Heaton, Haynes; Herschleb, Jill; Hindson, Christopher (April 2019). "Resolving the full spectrum of human genome variation using Linked-Reads". Genome Research. 29 (4): 635–645. doi:10.1101/gr.234443.118. ISSN 1088-9051. PMC 6442396. PMID 30894395.
Zheng, Grace X. Y.; Lau, Billy T.; Schnall-Levin, Michael; Jarosz, Mirna; Bell, John M.; Hindson, Christopher M.; Kyriazopoulou-Panagiotopoulou, Sofia; Masquelier, Donald A.; Merrill, Landon; Terry, Jessica M.; Mudivarti, Patrice A.; Wyatt, Paul W.; Bharadwaj, Rajiv; Makarewicz, Anthony J.; Li, Yuan (March 2016). "Haplotyping germline and cancer genomes with high-throughput linked-read sequencing". Nature Biotechnology. 34 (3): 303–311. doi:10.1038/nbt.3432. ISSN 1546-1696. PMC 4786454. PMID 26829319.
Mostovoy, Yulia; Levy-Sakin, Michal; Lam, Jessica; Lam, Ernest T; Hastie, Alex R; Marks, Patrick; Lee, Joyce; Chu, Catherine; Lin, Chin; Džakula, Željko; Cao, Han; Schlebusch, Stephen A; Giorda, Kristina; Schnall-Levin, Michael; Wall, Jeffrey D (July 2016). "A hybrid approach for de novo human genome sequence assembly and phasing". Nature Methods. 13 (7): 587–590. doi:10.1038/nmeth.3865. ISSN 1548-7091. PMC 4927370. PMID 27159086.
Elyanow, Rebecca; Wu, Hsin-Ta; Raphael, Benjamin J (2018-01-15). Curtis, Christina (ed.). "Identifying structural variants using linked-read sequencing data". Bioinformatics. 34 (2): 353–360. doi:10.1093/bioinformatics/btx712. ISSN 1367-4803. PMC 5860216. PMID 29112732.
Ott, Alina; Schnable, James C.; Yeh, Cheng-Ting; Wu, Linjiang; Liu, Chao; Hu, Heng-Cheng; Dalgard, Clifton L.; Sarkar, Soumik; Schnable, Patrick S. (2018-09-04). "Linked read technology for assembling large complex and polyploid genomes". BMC Genomics. 19 (1): 651. doi:10.1186/s12864-018-5040-z. ISSN 1471-2164. PMC 6122573. PMID 30180802.
Martinez-Viaud, Karine A; Lawley, Cindy Taylor; Vergara, Milmer Martinez; Ben-Zvi, Gil; Biniashvili, Tammy; Baruch, Kobi; St. Leger, Judy; Le, Jennie; Natarajan, Aparna; Rivera, Marlem; Guillergan, Marbie; Jaeger, Erich; Steffy, Brian; Zimin, Aleksey (2019-03-01). "New de novo assembly of the Atlantic bottlenose dolphin ( Tursiops truncatus ) improves genome completeness and provides haplotype phasing". GigaScience. 8 (3). doi:10.1093/gigascience/giy168. ISSN 2047-217X. PMC 6443575. PMID 30698692.
Wu, Shan; Lau, Kin H.; Cao, Qinghe; Hamilton, John P.; Sun, Honghe; Zhou, Chenxi; Eserman, Lauren; Gemenet, Dorcus C.; Olukolu, Bode A.; Wang, Haiyan; Crisovan, Emily; Godden, Grant T.; Jiao, Chen; Wang, Xin; Kitavi, Mercy (2018-11-02). "Genome sequences of two diploid wild relatives of cultivated sweetpotato reveal targets for genetic improvement". Nature Communications. 9 (1): 4580. Bibcode:2018NatCo...9.4580W. doi:10.1038/s41467-018-06983-8. ISSN 2041-1723. PMC 6214957. PMID 30389915.
Kronenberg, Zev N.; Fiddes, Ian T.; Gordon, David; Murali, Shwetha; Cantsilieris, Stuart; Meyerson, Olivia S.; Underwood, Jason G.; Nelson, Bradley J.; Chaisson, Mark J. P.; Dougherty, Max L.; Munson, Katherine M.; Hastie, Alex R.; Diekhans, Mark; Hormozdiari, Fereydoun; Lorusso, Nicola (2018-06-08). "High-resolution comparative analysis of great ape genomes". Science. 360 (6393): eaar6343. doi:10.1126/science.aar6343. ISSN 0036-8075. PMC 6178954. PMID 29880660.
Maestri, Simone; Maturo, Maria Giovanna; Cosentino, Emanuela; Marcolungo, Luca; Iadarola, Barbara; Fortunati, Elisabetta; Rossato, Marzia; Delledonne, Massimo (2020-12-01). "A Long-Read Sequencing Approach for Direct Haplotype Phasing in Clinical Settings". International Journal of Molecular Sciences. 21 (23): 9177. doi:10.3390/ijms21239177. ISSN 1422-0067. PMC 7731377. PMID 33271988.
Jang, Se Song; Lim, Byung Chan; Yoo, Seong-Keun; Shin, Jong-Yeon; Kim, Ki-Joong; Seo, Jeong-Sun; Kim, Jong-Il; Chae, Jong Hee (2018-06-06). "Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis". Scientific Reports. 8 (1): 8678. Bibcode:2018NatSR...8.8678J. doi:10.1038/s41598-018-26941-0. ISSN 2045-2322. PMC 5989205. PMID 29875376.
Ostendorf, Benjamin N.; Bilanovic, Jana; Adaku, Nneoma; Tafreshian, Kimia N.; Tavora, Bernardo; Vaughan, Roger D.; Tavazoie, Sohail F. (July 2020). "Common germline variants of the human APOE gene modulate melanoma progression and survival". Nature Medicine. 26 (7): 1048–1053. doi:10.1038/s41591-020-0879-3. ISSN 1546-170X. PMC 8058866. PMID 32451497.
Tilgner, Hagen; Jahanbani, Fereshteh; Gupta, Ishaan; Collier, Paul; Wei, Eric; Rasmussen, Morten; Snyder, Michael (February 2018). "Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome". Genome Research. 28 (2): 231–242. doi:10.1101/gr.230516.117. ISSN 1088-9051. PMC 5793787. PMID 29196558.
Konki, Mikko; Malonzo, Maia; Karlsson, Ida K.; Lindgren, Noora; Ghimire, Bishwa; Smolander, Johannes; Scheinin, Noora M.; Ollikainen, Miina; Laiho, Asta; Elo, Laura L.; Lönnberg, Tapio; Röyttä, Matias; Pedersen, Nancy L.; Kaprio, Jaakko; Lähdesmäki, Harri (December 2019). "Peripheral blood DNA methylation differences in twin pairs discordant for Alzheimer's disease". Clinical Epigenetics. 11 (1): 130. doi:10.1186/s13148-019-0729-7. ISSN 1868-7075. PMC 6721173. PMID 31477183.
McGrath-Morrow, Sharon A.; Ndeh, Roland; Helmin, Kathryn A.; Khuder, Basil; Rothblum-Oviatt, Cynthia; Collaco, Joseph M.; Wright, Jennifer; Reyfman, Paul A.; Lederman, Howard M.; Singer, Benjamin D. (2020-05-04). "DNA methylation and gene expression signatures are associated with ataxia-telangiectasia phenotype". Scientific Reports. 10 (1): 7479. Bibcode:2020NatSR..10.7479M. doi:10.1038/s41598-020-64514-2. ISSN 2045-2322. PMC 7198504. PMID 32366930.

harvard.edu

ui.adsabs.harvard.edu

Wu, Shan; Lau, Kin H.; Cao, Qinghe; Hamilton, John P.; Sun, Honghe; Zhou, Chenxi; Eserman, Lauren; Gemenet, Dorcus C.; Olukolu, Bode A.; Wang, Haiyan; Crisovan, Emily; Godden, Grant T.; Jiao, Chen; Wang, Xin; Kitavi, Mercy (2018-11-02). "Genome sequences of two diploid wild relatives of cultivated sweetpotato reveal targets for genetic improvement". Nature Communications. 9 (1): 4580. Bibcode:2018NatCo...9.4580W. doi:10.1038/s41467-018-06983-8. ISSN 2041-1723. PMC 6214957. PMID 30389915.
Jang, Se Song; Lim, Byung Chan; Yoo, Seong-Keun; Shin, Jong-Yeon; Kim, Ki-Joong; Seo, Jeong-Sun; Kim, Jong-Il; Chae, Jong Hee (2018-06-06). "Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis". Scientific Reports. 8 (1): 8678. Bibcode:2018NatSR...8.8678J. doi:10.1038/s41598-018-26941-0. ISSN 2045-2322. PMC 5989205. PMID 29875376.
McGrath-Morrow, Sharon A.; Ndeh, Roland; Helmin, Kathryn A.; Khuder, Basil; Rothblum-Oviatt, Cynthia; Collaco, Joseph M.; Wright, Jennifer; Reyfman, Paul A.; Lederman, Howard M.; Singer, Benjamin D. (2020-05-04). "DNA methylation and gene expression signatures are associated with ataxia-telangiectasia phenotype". Scientific Reports. 10 (1): 7479. Bibcode:2020NatSR..10.7479M. doi:10.1038/s41598-020-64514-2. ISSN 2045-2322. PMC 7198504. PMID 32366930.

justia.com

cases.justia.com

"United States Court of Appeals for the Federal Circuit - Bio-Rad Laboratories Inc. v. 10x Genomics" (PDF). Cases.Justia.com. 2020-08-03.

nih.gov

ncbi.nlm.nih.gov

Marks, Patrick; Garcia, Sarah; Barrio, Alvaro Martinez; Belhocine, Kamila; Bernate, Jorge; Bharadwaj, Rajiv; Bjornson, Keith; Catalanotti, Claudia; Delaney, Josh; Fehr, Adrian; Fiddes, Ian T.; Galvin, Brendan; Heaton, Haynes; Herschleb, Jill; Hindson, Christopher (April 2019). "Resolving the full spectrum of human genome variation using Linked-Reads". Genome Research. 29 (4): 635–645. doi:10.1101/gr.234443.118. ISSN 1088-9051. PMC 6442396. PMID 30894395.
Zheng, Grace X. Y.; Lau, Billy T.; Schnall-Levin, Michael; Jarosz, Mirna; Bell, John M.; Hindson, Christopher M.; Kyriazopoulou-Panagiotopoulou, Sofia; Masquelier, Donald A.; Merrill, Landon; Terry, Jessica M.; Mudivarti, Patrice A.; Wyatt, Paul W.; Bharadwaj, Rajiv; Makarewicz, Anthony J.; Li, Yuan (March 2016). "Haplotyping germline and cancer genomes with high-throughput linked-read sequencing". Nature Biotechnology. 34 (3): 303–311. doi:10.1038/nbt.3432. ISSN 1546-1696. PMC 4786454. PMID 26829319.
Mostovoy, Yulia; Levy-Sakin, Michal; Lam, Jessica; Lam, Ernest T; Hastie, Alex R; Marks, Patrick; Lee, Joyce; Chu, Catherine; Lin, Chin; Džakula, Željko; Cao, Han; Schlebusch, Stephen A; Giorda, Kristina; Schnall-Levin, Michael; Wall, Jeffrey D (July 2016). "A hybrid approach for de novo human genome sequence assembly and phasing". Nature Methods. 13 (7): 587–590. doi:10.1038/nmeth.3865. ISSN 1548-7091. PMC 4927370. PMID 27159086.
Elyanow, Rebecca; Wu, Hsin-Ta; Raphael, Benjamin J (2018-01-15). Curtis, Christina (ed.). "Identifying structural variants using linked-read sequencing data". Bioinformatics. 34 (2): 353–360. doi:10.1093/bioinformatics/btx712. ISSN 1367-4803. PMC 5860216. PMID 29112732.
Ott, Alina; Schnable, James C.; Yeh, Cheng-Ting; Wu, Linjiang; Liu, Chao; Hu, Heng-Cheng; Dalgard, Clifton L.; Sarkar, Soumik; Schnable, Patrick S. (2018-09-04). "Linked read technology for assembling large complex and polyploid genomes". BMC Genomics. 19 (1): 651. doi:10.1186/s12864-018-5040-z. ISSN 1471-2164. PMC 6122573. PMID 30180802.
Martinez-Viaud, Karine A; Lawley, Cindy Taylor; Vergara, Milmer Martinez; Ben-Zvi, Gil; Biniashvili, Tammy; Baruch, Kobi; St. Leger, Judy; Le, Jennie; Natarajan, Aparna; Rivera, Marlem; Guillergan, Marbie; Jaeger, Erich; Steffy, Brian; Zimin, Aleksey (2019-03-01). "New de novo assembly of the Atlantic bottlenose dolphin ( Tursiops truncatus ) improves genome completeness and provides haplotype phasing". GigaScience. 8 (3). doi:10.1093/gigascience/giy168. ISSN 2047-217X. PMC 6443575. PMID 30698692.
Wu, Shan; Lau, Kin H.; Cao, Qinghe; Hamilton, John P.; Sun, Honghe; Zhou, Chenxi; Eserman, Lauren; Gemenet, Dorcus C.; Olukolu, Bode A.; Wang, Haiyan; Crisovan, Emily; Godden, Grant T.; Jiao, Chen; Wang, Xin; Kitavi, Mercy (2018-11-02). "Genome sequences of two diploid wild relatives of cultivated sweetpotato reveal targets for genetic improvement". Nature Communications. 9 (1): 4580. Bibcode:2018NatCo...9.4580W. doi:10.1038/s41467-018-06983-8. ISSN 2041-1723. PMC 6214957. PMID 30389915.
Kronenberg, Zev N.; Fiddes, Ian T.; Gordon, David; Murali, Shwetha; Cantsilieris, Stuart; Meyerson, Olivia S.; Underwood, Jason G.; Nelson, Bradley J.; Chaisson, Mark J. P.; Dougherty, Max L.; Munson, Katherine M.; Hastie, Alex R.; Diekhans, Mark; Hormozdiari, Fereydoun; Lorusso, Nicola (2018-06-08). "High-resolution comparative analysis of great ape genomes". Science. 360 (6393): eaar6343. doi:10.1126/science.aar6343. ISSN 0036-8075. PMC 6178954. PMID 29880660.
Maestri, Simone; Maturo, Maria Giovanna; Cosentino, Emanuela; Marcolungo, Luca; Iadarola, Barbara; Fortunati, Elisabetta; Rossato, Marzia; Delledonne, Massimo (2020-12-01). "A Long-Read Sequencing Approach for Direct Haplotype Phasing in Clinical Settings". International Journal of Molecular Sciences. 21 (23): 9177. doi:10.3390/ijms21239177. ISSN 1422-0067. PMC 7731377. PMID 33271988.
Jang, Se Song; Lim, Byung Chan; Yoo, Seong-Keun; Shin, Jong-Yeon; Kim, Ki-Joong; Seo, Jeong-Sun; Kim, Jong-Il; Chae, Jong Hee (2018-06-06). "Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis". Scientific Reports. 8 (1): 8678. Bibcode:2018NatSR...8.8678J. doi:10.1038/s41598-018-26941-0. ISSN 2045-2322. PMC 5989205. PMID 29875376.
Ostendorf, Benjamin N.; Bilanovic, Jana; Adaku, Nneoma; Tafreshian, Kimia N.; Tavora, Bernardo; Vaughan, Roger D.; Tavazoie, Sohail F. (July 2020). "Common germline variants of the human APOE gene modulate melanoma progression and survival". Nature Medicine. 26 (7): 1048–1053. doi:10.1038/s41591-020-0879-3. ISSN 1546-170X. PMC 8058866. PMID 32451497.
Tilgner, Hagen; Jahanbani, Fereshteh; Gupta, Ishaan; Collier, Paul; Wei, Eric; Rasmussen, Morten; Snyder, Michael (February 2018). "Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome". Genome Research. 28 (2): 231–242. doi:10.1101/gr.230516.117. ISSN 1088-9051. PMC 5793787. PMID 29196558.
Konki, Mikko; Malonzo, Maia; Karlsson, Ida K.; Lindgren, Noora; Ghimire, Bishwa; Smolander, Johannes; Scheinin, Noora M.; Ollikainen, Miina; Laiho, Asta; Elo, Laura L.; Lönnberg, Tapio; Röyttä, Matias; Pedersen, Nancy L.; Kaprio, Jaakko; Lähdesmäki, Harri (December 2019). "Peripheral blood DNA methylation differences in twin pairs discordant for Alzheimer's disease". Clinical Epigenetics. 11 (1): 130. doi:10.1186/s13148-019-0729-7. ISSN 1868-7075. PMC 6721173. PMID 31477183.
McGrath-Morrow, Sharon A.; Ndeh, Roland; Helmin, Kathryn A.; Khuder, Basil; Rothblum-Oviatt, Cynthia; Collaco, Joseph M.; Wright, Jennifer; Reyfman, Paul A.; Lederman, Howard M.; Singer, Benjamin D. (2020-05-04). "DNA methylation and gene expression signatures are associated with ataxia-telangiectasia phenotype". Scientific Reports. 10 (1): 7479. Bibcode:2020NatSR..10.7479M. doi:10.1038/s41598-020-64514-2. ISSN 2045-2322. PMC 7198504. PMID 32366930.

pubmed.ncbi.nlm.nih.gov

Marks, Patrick; Garcia, Sarah; Barrio, Alvaro Martinez; Belhocine, Kamila; Bernate, Jorge; Bharadwaj, Rajiv; Bjornson, Keith; Catalanotti, Claudia; Delaney, Josh; Fehr, Adrian; Fiddes, Ian T.; Galvin, Brendan; Heaton, Haynes; Herschleb, Jill; Hindson, Christopher (April 2019). "Resolving the full spectrum of human genome variation using Linked-Reads". Genome Research. 29 (4): 635–645. doi:10.1101/gr.234443.118. ISSN 1088-9051. PMC 6442396. PMID 30894395.
Zheng, Grace X. Y.; Lau, Billy T.; Schnall-Levin, Michael; Jarosz, Mirna; Bell, John M.; Hindson, Christopher M.; Kyriazopoulou-Panagiotopoulou, Sofia; Masquelier, Donald A.; Merrill, Landon; Terry, Jessica M.; Mudivarti, Patrice A.; Wyatt, Paul W.; Bharadwaj, Rajiv; Makarewicz, Anthony J.; Li, Yuan (March 2016). "Haplotyping germline and cancer genomes with high-throughput linked-read sequencing". Nature Biotechnology. 34 (3): 303–311. doi:10.1038/nbt.3432. ISSN 1546-1696. PMC 4786454. PMID 26829319.
Mostovoy, Yulia; Levy-Sakin, Michal; Lam, Jessica; Lam, Ernest T; Hastie, Alex R; Marks, Patrick; Lee, Joyce; Chu, Catherine; Lin, Chin; Džakula, Željko; Cao, Han; Schlebusch, Stephen A; Giorda, Kristina; Schnall-Levin, Michael; Wall, Jeffrey D (July 2016). "A hybrid approach for de novo human genome sequence assembly and phasing". Nature Methods. 13 (7): 587–590. doi:10.1038/nmeth.3865. ISSN 1548-7091. PMC 4927370. PMID 27159086.
Elyanow, Rebecca; Wu, Hsin-Ta; Raphael, Benjamin J (2018-01-15). Curtis, Christina (ed.). "Identifying structural variants using linked-read sequencing data". Bioinformatics. 34 (2): 353–360. doi:10.1093/bioinformatics/btx712. ISSN 1367-4803. PMC 5860216. PMID 29112732.
Ott, Alina; Schnable, James C.; Yeh, Cheng-Ting; Wu, Linjiang; Liu, Chao; Hu, Heng-Cheng; Dalgard, Clifton L.; Sarkar, Soumik; Schnable, Patrick S. (2018-09-04). "Linked read technology for assembling large complex and polyploid genomes". BMC Genomics. 19 (1): 651. doi:10.1186/s12864-018-5040-z. ISSN 1471-2164. PMC 6122573. PMID 30180802.
Martinez-Viaud, Karine A; Lawley, Cindy Taylor; Vergara, Milmer Martinez; Ben-Zvi, Gil; Biniashvili, Tammy; Baruch, Kobi; St. Leger, Judy; Le, Jennie; Natarajan, Aparna; Rivera, Marlem; Guillergan, Marbie; Jaeger, Erich; Steffy, Brian; Zimin, Aleksey (2019-03-01). "New de novo assembly of the Atlantic bottlenose dolphin ( Tursiops truncatus ) improves genome completeness and provides haplotype phasing". GigaScience. 8 (3). doi:10.1093/gigascience/giy168. ISSN 2047-217X. PMC 6443575. PMID 30698692.
Wu, Shan; Lau, Kin H.; Cao, Qinghe; Hamilton, John P.; Sun, Honghe; Zhou, Chenxi; Eserman, Lauren; Gemenet, Dorcus C.; Olukolu, Bode A.; Wang, Haiyan; Crisovan, Emily; Godden, Grant T.; Jiao, Chen; Wang, Xin; Kitavi, Mercy (2018-11-02). "Genome sequences of two diploid wild relatives of cultivated sweetpotato reveal targets for genetic improvement". Nature Communications. 9 (1): 4580. Bibcode:2018NatCo...9.4580W. doi:10.1038/s41467-018-06983-8. ISSN 2041-1723. PMC 6214957. PMID 30389915.
Kronenberg, Zev N.; Fiddes, Ian T.; Gordon, David; Murali, Shwetha; Cantsilieris, Stuart; Meyerson, Olivia S.; Underwood, Jason G.; Nelson, Bradley J.; Chaisson, Mark J. P.; Dougherty, Max L.; Munson, Katherine M.; Hastie, Alex R.; Diekhans, Mark; Hormozdiari, Fereydoun; Lorusso, Nicola (2018-06-08). "High-resolution comparative analysis of great ape genomes". Science. 360 (6393): eaar6343. doi:10.1126/science.aar6343. ISSN 0036-8075. PMC 6178954. PMID 29880660.
Maestri, Simone; Maturo, Maria Giovanna; Cosentino, Emanuela; Marcolungo, Luca; Iadarola, Barbara; Fortunati, Elisabetta; Rossato, Marzia; Delledonne, Massimo (2020-12-01). "A Long-Read Sequencing Approach for Direct Haplotype Phasing in Clinical Settings". International Journal of Molecular Sciences. 21 (23): 9177. doi:10.3390/ijms21239177. ISSN 1422-0067. PMC 7731377. PMID 33271988.
Jang, Se Song; Lim, Byung Chan; Yoo, Seong-Keun; Shin, Jong-Yeon; Kim, Ki-Joong; Seo, Jeong-Sun; Kim, Jong-Il; Chae, Jong Hee (2018-06-06). "Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis". Scientific Reports. 8 (1): 8678. Bibcode:2018NatSR...8.8678J. doi:10.1038/s41598-018-26941-0. ISSN 2045-2322. PMC 5989205. PMID 29875376.
Ostendorf, Benjamin N.; Bilanovic, Jana; Adaku, Nneoma; Tafreshian, Kimia N.; Tavora, Bernardo; Vaughan, Roger D.; Tavazoie, Sohail F. (July 2020). "Common germline variants of the human APOE gene modulate melanoma progression and survival". Nature Medicine. 26 (7): 1048–1053. doi:10.1038/s41591-020-0879-3. ISSN 1546-170X. PMC 8058866. PMID 32451497.
Tilgner, Hagen; Jahanbani, Fereshteh; Gupta, Ishaan; Collier, Paul; Wei, Eric; Rasmussen, Morten; Snyder, Michael (February 2018). "Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome". Genome Research. 28 (2): 231–242. doi:10.1101/gr.230516.117. ISSN 1088-9051. PMC 5793787. PMID 29196558.
Konki, Mikko; Malonzo, Maia; Karlsson, Ida K.; Lindgren, Noora; Ghimire, Bishwa; Smolander, Johannes; Scheinin, Noora M.; Ollikainen, Miina; Laiho, Asta; Elo, Laura L.; Lönnberg, Tapio; Röyttä, Matias; Pedersen, Nancy L.; Kaprio, Jaakko; Lähdesmäki, Harri (December 2019). "Peripheral blood DNA methylation differences in twin pairs discordant for Alzheimer's disease". Clinical Epigenetics. 11 (1): 130. doi:10.1186/s13148-019-0729-7. ISSN 1868-7075. PMC 6721173. PMID 31477183.
McGrath-Morrow, Sharon A.; Ndeh, Roland; Helmin, Kathryn A.; Khuder, Basil; Rothblum-Oviatt, Cynthia; Collaco, Joseph M.; Wright, Jennifer; Reyfman, Paul A.; Lederman, Howard M.; Singer, Benjamin D. (2020-05-04). "DNA methylation and gene expression signatures are associated with ataxia-telangiectasia phenotype". Scientific Reports. 10 (1): 7479. Bibcode:2020NatSR..10.7479M. doi:10.1038/s41598-020-64514-2. ISSN 2045-2322. PMC 7198504. PMID 32366930.

oup.com

academic.oup.com

Elyanow, Rebecca; Wu, Hsin-Ta; Raphael, Benjamin J (2018-01-15). Curtis, Christina (ed.). "Identifying structural variants using linked-read sequencing data". Bioinformatics. 34 (2): 353–360. doi:10.1093/bioinformatics/btx712. ISSN 1367-4803. PMC 5860216. PMID 29112732.

worldcat.org

search.worldcat.org

Marks, Patrick; Garcia, Sarah; Barrio, Alvaro Martinez; Belhocine, Kamila; Bernate, Jorge; Bharadwaj, Rajiv; Bjornson, Keith; Catalanotti, Claudia; Delaney, Josh; Fehr, Adrian; Fiddes, Ian T.; Galvin, Brendan; Heaton, Haynes; Herschleb, Jill; Hindson, Christopher (April 2019). "Resolving the full spectrum of human genome variation using Linked-Reads". Genome Research. 29 (4): 635–645. doi:10.1101/gr.234443.118. ISSN 1088-9051. PMC 6442396. PMID 30894395.
Zheng, Grace X. Y.; Lau, Billy T.; Schnall-Levin, Michael; Jarosz, Mirna; Bell, John M.; Hindson, Christopher M.; Kyriazopoulou-Panagiotopoulou, Sofia; Masquelier, Donald A.; Merrill, Landon; Terry, Jessica M.; Mudivarti, Patrice A.; Wyatt, Paul W.; Bharadwaj, Rajiv; Makarewicz, Anthony J.; Li, Yuan (March 2016). "Haplotyping germline and cancer genomes with high-throughput linked-read sequencing". Nature Biotechnology. 34 (3): 303–311. doi:10.1038/nbt.3432. ISSN 1546-1696. PMC 4786454. PMID 26829319.
Mostovoy, Yulia; Levy-Sakin, Michal; Lam, Jessica; Lam, Ernest T; Hastie, Alex R; Marks, Patrick; Lee, Joyce; Chu, Catherine; Lin, Chin; Džakula, Željko; Cao, Han; Schlebusch, Stephen A; Giorda, Kristina; Schnall-Levin, Michael; Wall, Jeffrey D (July 2016). "A hybrid approach for de novo human genome sequence assembly and phasing". Nature Methods. 13 (7): 587–590. doi:10.1038/nmeth.3865. ISSN 1548-7091. PMC 4927370. PMID 27159086.
Elyanow, Rebecca; Wu, Hsin-Ta; Raphael, Benjamin J (2018-01-15). Curtis, Christina (ed.). "Identifying structural variants using linked-read sequencing data". Bioinformatics. 34 (2): 353–360. doi:10.1093/bioinformatics/btx712. ISSN 1367-4803. PMC 5860216. PMID 29112732.
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