-
1
-
-
78649265888
-
Ovarian cancer biomarkers for molecular biosensors and translational medicine
-
PMID: 21080822
-
Suh KS, Park SW, Castro A, Patel H, Blake P, Liang M, et al. Ovarian cancer biomarkers for molecular biosensors and translational medicine. Expert review of molecular diagnostics. 2010; 10(8):1069–83. https://doi.org/10.1586/erm.10.87 PMID: 21080822.
-
(2010)
Expert Review of Molecular Diagnostics
, vol.10
, Issue.8
, pp. 1069-1083
-
-
Suh, K.S.1
Park, S.W.2
Castro, A.3
Patel, H.4
Blake, P.5
Liang, M.6
-
2
-
-
63149087256
-
Sensitivity and specificity of multimodal and ultrasound screening for ovarian cancer, and stage distribution of detected cancers: Results of the prevalence screen of the UK collaborative trial of ovarian cancer screening (UKc-tocs)
-
PMID:19282241
-
Menon U, Gentry-Maharaj A, Hallett R, Ryan A, Burnell M, Sharma A, et al. Sensitivity and specificity of multimodal and ultrasound screening for ovarian cancer, and stage distribution of detected cancers: results of the prevalence screen of the UK Collaborative Trial of Ovarian Cancer Screening (UKC-TOCS). The Lancet Oncology. 2009; 10(4):327–40. https://doi.org/10.1016/S1470-2045(09)70026-9PMID: 19282241.
-
(2009)
The Lancet Oncology
, vol.10
, Issue.4
, pp. 327-340
-
-
Menon, U.1
Gentry-Maharaj, A.2
Hallett, R.3
Ryan, A.4
Burnell, M.5
Sharma, A.6
-
3
-
-
80054739549
-
Cumulative probability of false-positive recall or biopsy recommendation after 10 years of screening mammography: A cohort study
-
PMID: 22007042; PubMed Central PMCID: PMC3209800
-
Hubbard RA, Kerlikowske K, Flowers CI, Yankaskas BC, Zhu W, Miglioretti DL. Cumulative probability of false-positive recall or biopsy recommendation after 10 years of screening mammography: a cohort study. Annals of internal medicine. 2011; 155(8):481–92. https://doi.org/10.7326/0003-4819-155-8-201110180-00004 PMID: 22007042; PubMed Central PMCID: PMC3209800.
-
(2011)
Annals of Internal Medicine
, vol.155
, Issue.8
, pp. 481-492
-
-
Hubbard, R.A.1
Kerlikowske, K.2
Flowers, C.I.3
Yankaskas, B.C.4
Zhu, W.5
Miglioretti, D.L.6
-
4
-
-
84897509377
-
Multitarget stool DNA testing for colorectal-cancer screening
-
PMID: 24645800
-
Imperiale TF, Ransohoff DF, Itzkowitz SH, Levin TR, Lavin P, Lidgard GP, et al. Multitarget stool DNA testing for colorectal-cancer screening. The New England journal of medicine. 2014; 370(14):1287–97. https://doi.org/10.1056/NEJMoa1311194 PMID: 24645800.
-
(2014)
The New England Journal of Medicine
, vol.370
, Issue.14
, pp. 1287-1297
-
-
Imperiale, T.F.1
Ransohoff, D.F.2
Itzkowitz, S.H.3
Levin, T.R.4
Lavin, P.5
Lidgard, G.P.6
-
5
-
-
0038497523
-
Effect of verification bias on screening for prostate cancer by measurement of prostate-specific antigen
-
PMID: 12878740
-
Punglia RS, D’Amico AV, Catalona WJ, Roehl KA, Kuntz KM. Effect of verification bias on screening for prostate cancer by measurement of prostate-specific antigen. The New England journal of medicine. 2003; 349(4):335–42. https://doi.org/10.1056/NEJMoa021659 PMID: 12878740.
-
(2003)
The New England Journal of Medicine
, vol.349
, Issue.4
, pp. 335-342
-
-
Punglia, R.S.1
D’Amico, A.V.2
Catalona, W.J.3
Roehl, K.A.4
Kuntz, K.M.5
-
6
-
-
79958036419
-
Effect of screening on ovarian cancer mortality: The prostate, lung, colorectal and ovarian (plco) cancer screening randomized controlled trial
-
PMID: 21642681
-
Buys SS, Partridge E, Black A, Johnson CC, Lamerato L, Isaacs C, et al. Effect of screening on ovarian cancer mortality: the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Randomized Controlled Trial. JAMA. 2011; 305(22):2295–303. https://doi.org/10.1001/jama.2011.766 PMID: 21642681.
-
(2011)
JAMA
, vol.305
, Issue.22
, pp. 2295-2303
-
-
Buys, S.S.1
Partridge, E.2
Black, A.3
Johnson, C.C.4
Lamerato, L.5
Isaacs, C.6
-
7
-
-
84903218109
-
An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage
-
PMID: 24705333; PubMed Central PMCID: PMCPMC4016134
-
Newman AM, Bratman SV, To J, Wynne JF, Eclov NC, Modlin LA, et al. An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. Nature medicine. 2014; 20(5):548–54. https://doi.org/10.1038/nm.3519 PMID: 24705333; PubMed Central PMCID: PMCPMC4016134.
-
(2014)
Nature Medicine
, vol.20
, Issue.5
, pp. 548-554
-
-
Newman, A.M.1
Bratman, S.V.2
To, J.3
Wynne, J.F.4
Eclov, N.C.5
Modlin, L.A.6
-
8
-
-
84875520648
-
Analysis of circulating tumor DNA to monitor metastatic breast cancer
-
PMID: 23484797
-
Dawson SJ, Tsui DW, Murtaza M, Biggs H, Rueda OM, Chin SF, et al. Analysis of circulating tumor DNA to monitor metastatic breast cancer. The New England journal of medicine. 2013; 368(13):1199–209. https://doi.org/10.1056/NEJMoa1213261 PMID: 23484797.
-
(2013)
The New England Journal of Medicine
, vol.368
, Issue.13
, pp. 1199-1209
-
-
Dawson, S.J.1
Tsui, D.W.2
Murtaza, M.3
Biggs, H.4
Rueda, O.M.5
Chin, S.F.6
-
9
-
-
84896371874
-
Detection of circulating tumor DNA in early- and late-stage human malignancies
-
PMID: 24553385; PubMed Central PMCID: PMCPMC4017867
-
Bettegowda C, Sausen M, Leary RJ, Kinde I, Wang Y, Agrawal N, et al. Detection of circulating tumor DNA in early- and late-stage human malignancies. Science translational medicine. 2014; 6 (224):224ra24. https://doi.org/10.1126/scitranslmed.3007094 PMID: 24553385; PubMed Central PMCID: PMCPMC4017867.
-
(2014)
Science Translational Medicine
, vol.6
, Issue.224
-
-
Bettegowda, C.1
Sausen, M.2
Leary, R.J.3
Kinde, I.4
Wang, Y.5
Agrawal, N.6
-
10
-
-
84881479047
-
Liquid biopsy: Monitoring cancer-genetics in the blood
-
PMID: 23836314
-
Crowley E, Di Nicolantonio F, Loupakis F, Bardelli A. Liquid biopsy: monitoring cancer-genetics in the blood. Nat Rev Clin Oncol. 2013; 10(8):472–84. https://doi.org/10.1038/nrclinonc.2013.110 PMID: 23836314.
-
(2013)
Nat Rev Clin Oncol
, vol.10
, Issue.8
, pp. 472-484
-
-
Crowley, E.1
Di Nicolantonio, F.2
Loupakis, F.3
Bardelli, A.4
-
11
-
-
84906827268
-
The dynamic range of circulating tumor DNA in metastatic breast cancer
-
PMID: 25107527; PubMed Central PMCID: PMCPMC4303230
-
Heidary M, Auer M, Ulz P, Heitzer E, Petru E, Gasch C, et al. The dynamic range of circulating tumor DNA in metastatic breast cancer. Breast Cancer Res. 2014; 16(4):421. https://doi.org/10.1186/s13058-014-0421-y PMID: 25107527; PubMed Central PMCID: PMCPMC4303230.
-
(2014)
Breast Cancer Res
, vol.16
, Issue.4
, pp. 421
-
-
Heidary, M.1
Auer, M.2
Ulz, P.3
Heitzer, E.4
Petru, E.5
Gasch, C.6
-
12
-
-
84872020299
-
Cancer genome scanning in plasma: Detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing
-
PMID: 23065472
-
Chan KC, Jiang P, Zheng YW, Liao GJ, Sun H, Wong J, et al. Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing. Clin Chem. 2013; 59(1):211–24. https://doi.org/10.1373/clinchem.2012.196014 PMID: 23065472.
-
(2013)
Clin Chem
, vol.59
, Issue.1
, pp. 211-224
-
-
Chan, K.C.1
Jiang, P.2
Zheng, Y.W.3
Liao, G.J.4
Sun, H.5
Wong, J.6
-
13
-
-
84870312106
-
Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing
-
PMID: 23197571; PubMed Central PMCID: PMC3641759
-
Leary RJ, Sausen M, Kinde I, Papadopoulos N, Carpten JD, Craig D, et al. Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing. Science translational medicine. 2012; 4(162):162ra54. https://doi.org/10.1126/scitranslmed.3004742 PMID: 23197571; PubMed Central PMCID: PMC3641759.
-
(2012)
Science Translational Medicine
, vol.4
, Issue.162
-
-
Leary, R.J.1
Sausen, M.2
Kinde, I.3
Papadopoulos, N.4
Carpten, J.D.5
Craig, D.6
-
14
-
-
76249088426
-
Copy number variations and cancer
-
PMID: 19566914; PubMed Central PMCID: PMC2703871
-
Shlien A, Malkin D. Copy number variations and cancer. Genome medicine. 2009; 1(6):62. https://doi.org/10.1186/gm62 PMID: 19566914; PubMed Central PMCID: PMC2703871.
-
(2009)
Genome Medicine
, vol.1
, Issue.6
, pp. 62
-
-
Shlien, A.1
Malkin, D.2
-
15
-
-
84885735554
-
Mutational landscape and significance across 12 major cancer types
-
PMID: 24132290 PubMed Central PMCID: PMC3927368
-
Kandoth C, McLellan MD, Vandin F, Ye K, Niu B, Lu C, et al. Mutational landscape and significance across 12 major cancer types. Nature. 2013; 502(7471):333–9. https://doi.org/10.1038/nature12634PMID: 24132290; PubMed Central PMCID: PMC3927368.
-
(2013)
Nature
, vol.502
, Issue.7471
, pp. 333-339
-
-
Kandoth, C.1
McLellan, M.D.2
Vandin, F.3
Ye, K.4
Niu, B.5
Lu, C.6
-
16
-
-
33645769276
-
High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients
-
PMID: 16616336
-
Carrasco DR, Tonon G, Huang Y, Zhang Y, Sinha R, Feng B, et al. High-resolution genomic profiles define distinct clinico-pathogenetic subgroups of multiple myeloma patients. Cancer Cell. 2006; 9 (4):313–25. https://doi.org/10.1016/j.ccr.2006.03.019 PMID: 16616336.
-
(2006)
Cancer Cell
, vol.9
, Issue.4
, pp. 313-325
-
-
Carrasco, D.R.1
Tonon, G.2
Huang, Y.3
Zhang, Y.4
Sinha, R.5
Feng, B.6
-
17
-
-
84908460595
-
Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin
-
PMID: 25109877; PubMed Central PMCID: PMC4152462
-
Hoadley KA, Yau C, Wolf DM, Cherniack AD, Tamborero D, Ng S, et al. Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin. Cell. 2014; 158 (4):929–44. https://doi.org/10.1016/j.cell.2014.06.049 PMID: 25109877; PubMed Central PMCID: PMC4152462.
-
(2014)
Cell
, vol.158
, Issue.4
, pp. 929-944
-
-
Hoadley, K.A.1
Yau, C.2
Wolf, D.M.3
Cherniack, A.D.4
Tamborero, D.5
Ng, S.6
-
18
-
-
84887084951
-
Network-based stratification of tumor mutations
-
PMID: 24037242; PubMed Central PMCID: PMCPMC3866081
-
Hofree M, Shen JP, Carter H, Gross A, Ideker T. Network-based stratification of tumor mutations. Nature methods. 2013; 10(11):1108–15. https://doi.org/10.1038/nmeth.2651 PMID: 24037242; PubMed Central PMCID: PMCPMC3866081.
-
(2013)
Nature Methods
, vol.10
, Issue.11
, pp. 1108-1115
-
-
Hofree, M.1
Shen, J.P.2
Carter, H.3
Gross, A.4
Ideker, T.5
-
19
-
-
84875824898
-
Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing
-
PMID: 23561577; PubMed Central PMCID: PMCPMC3707016
-
Heitzer E, Ulz P, Belic J, Gutschi S, Quehenberger F, Fischereder K, et al. Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing. Genome medicine. 2013; 5(4):30. https://doi.org/10.1186/gm434 PMID: 23561577; PubMed Central PMCID: PMCPMC3707016.
-
(2013)
Genome Medicine
, vol.5
, Issue.4
, pp. 30
-
-
Heitzer, E.1
Ulz, P.2
Belic, J.3
Gutschi, S.4
Quehenberger, F.5
Fischereder, K.6
-
20
-
-
85022337999
-
Detection of clonal and subclonal
-
Kirkizlar E, Zimmermann B, Constantin T, Swenerton R, Hoang B, Wayham N, et al. Detection of Clonal and Subclonal Copy-Number Variants in Cell-Free DNA from Patients with Breast Cancer Using a
-
Copy-number Variants in Cell-free DNA from Patients with Breast Cancer Using A
-
-
Kirkizlar, E.1
Zimmermann, B.2
Constantin, T.3
Swenerton, R.4
Hoang, B.5
Wayham, N.6
-
21
-
-
84945925969
-
Massively multiplexed PCR methodology
-
PMID: 26500031; PubMed Central PMCID: PMCPMC4631096
-
Massively Multiplexed PCR Methodology. Transl Oncol. 2015; 8(5):407–16. https://doi.org/10.1016/j.tranon.2015.08.004 PMID: 26500031; PubMed Central PMCID: PMCPMC4631096.
-
(2015)
Transl Oncol
, vol.8
, Issue.5
, pp. 407-416
-
-
-
22
-
-
84937459187
-
Noninvasive prenatal testing and incidental detection of occult maternal malignancies
-
PMID: 26168314
-
Bianchi DW, Chudova D, Sehnert AJ, Bhatt S, Murray K, Prosen TL, et al. Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies. JAMA. 2015; 314(2):162–9. https://doi.org/10.1001/jama.2015.7120 PMID: 26168314.
-
(2015)
JAMA
, vol.314
, Issue.2
, pp. 162-169
-
-
Bianchi, D.W.1
Chudova, D.2
Sehnert, A.J.3
Bhatt, S.4
Murray, K.5
Prosen, T.L.6
-
23
-
-
84943394447
-
Presymptomatic identification of cancers in pregnant women during noninvasive prenatal testing
-
PMID:26355862
-
Amant F, Verheecke M, Wlodarska I, Dehaspe L, Brady P, Brison N, et al. Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing. JAMA Oncol. 2015; 1 (6):814–9. https://doi.org/10.1001/jamaoncol.2015.1883 PMID: 26355862.
-
(2015)
JAMA Oncol
, vol.1
, Issue.6
, pp. 814-819
-
-
Amant, F.1
Verheecke, M.2
Wlodarska, I.3
Dehaspe, L.4
Brady, P.5
Brison, N.6
-
24
-
-
84961857091
-
Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants
-
PMID: 26899906
-
Lefkowitz RB, Tynan JA, Liu T, Wu Y, Mazloom AR, Almasri E, et al. Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants. Am J Obstet Gynecol. 2016. https://doi.org/10.1016/j.ajog.2016.02.030 PMID: 26899906.
-
(2016)
Am J Obstet Gynecol
-
-
Lefkowitz, R.B.1
Tynan, J.A.2
Liu, T.3
Wu, Y.4
Mazloom, A.R.5
Almasri, E.6
-
25
-
-
77957736539
-
Quantification of fetal DNA by use of methylation-based DNA discrimination
-
PMID: 20729299
-
Nygren AOH, Dean J, Jensen TJ, Kruse S, Kwong W, van den Boom D, et al. Quantification of Fetal DNA by Use of Methylation-Based DNA Discrimination. Clinical Chemistry. 2010; 56(10):1627–35. https://doi.org/10.1373/clinchem.2010.146290 PMID: 20729299
-
(2010)
Clinical Chemistry
, vol.56
, Issue.10
, pp. 1627-1635
-
-
Nygren, A.O.H.1
Dean, J.2
Jensen, T.J.3
Kruse, S.4
Kwong, W.5
van Den Boom, D.6
-
26
-
-
84863954202
-
Non-invasive prenatal measurement of the fetal genome
-
PMID: 22763444; PubMed Central PMCID: PMC3561905
-
Fan HC, Gu W, Wang J, Blumenfeld YJ, El-Sayed YY, Quake SR. Non-invasive prenatal measurement of the fetal genome. Nature. 2012; 487(7407):320–4. https://doi.org/10.1038/nature11251 PMID: 22763444; PubMed Central PMCID: PMC3561905.
-
(2012)
Nature
, vol.487
, Issue.7407
, pp. 320-324
-
-
Fan, H.C.1
Gu, W.2
Wang, J.3
Blumenfeld, Y.J.4
El-Sayed, Y.Y.5
Quake, S.R.6
-
27
-
-
84885008220
-
Pan-cancer patterns of somatic copy number alteration
-
PMID: 24071852; PubMed Central PMCID: PMC3966983
-
Zack TI, Schumacher SE, Carter SL, Cherniack AD, Saksena G, Tabak B, et al. Pan-cancer patterns of somatic copy number alteration. Nature genetics. 2013; 45(10):1134–40. https://doi.org/10.1038/ng. 2760 PMID: 24071852; PubMed Central PMCID: PMC3966983.
-
(2013)
Nature Genetics
, vol.45
, Issue.10
, pp. 1134-1140
-
-
Zack, T.I.1
Schumacher, S.E.2
Carter, S.L.3
Cherniack, A.D.4
Saksena, G.5
Tabak, B.6
-
28
-
-
77249119762
-
The landscape of somatic copy-number alteration across human cancers
-
PMID: 20164920; PubMed Central PMCID: PMCPMC2826709
-
Beroukhim R, Mermel CH, Porter D, Wei G, Raychaudhuri S, Donovan J, et al. The landscape of somatic copy-number alteration across human cancers. Nature. 2010; 463(7283):899–905. https://doi.org/10.1038/nature08822 PMID: 20164920; PubMed Central PMCID: PMCPMC2826709.
-
(2010)
Nature
, vol.463
, Issue.7283
, pp. 899-905
-
-
Beroukhim, R.1
Mermel, C.H.2
Porter, D.3
Wei, G.4
Raychaudhuri, S.5
Donovan, J.6
-
30
-
-
84884997982
-
Emerging landscape of onco-genic signatures across human cancers
-
PMID: 24071851; PubMed Central PMCID: PMC4320046
-
Ciriello G, Miller ML, Aksoy BA, Senbabaoglu Y, Schultz N, Sander C. Emerging landscape of onco-genic signatures across human cancers. Nature genetics. 2013; 45(10):1127–33. https://doi.org/10.1038/ng.2762 PMID: 24071851; PubMed Central PMCID: PMC4320046.
-
(2013)
Nature Genetics
, vol.45
, Issue.10
, pp. 1127-1133
-
-
Ciriello, G.1
Miller, M.L.2
Aksoy, B.A.3
Senbabaoglu, Y.4
Schultz, N.5
Sander, C.6
-
31
-
-
0023181644
-
Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma
-
PMID: 2885753
-
Zbar B, Brauch H, Talmadge C, Linehan M. Loss of alleles of loci on the short arm of chromosome 3 in renal cell carcinoma. Nature. 1987; 327(6124):721–4. https://doi.org/10.1038/327721a0 PMID: 2885753.
-
(1987)
Nature
, vol.327
, Issue.6124
, pp. 721-724
-
-
Zbar, B.1
Brauch, H.2
Talmadge, C.3
Linehan, M.4
-
32
-
-
84905049901
-
Trimmomatic: A flexible trimmer for illumina sequence data
-
PMID: 24695404; PubMed Central PMCID: PMCPMC4103590
-
Bolger AM, Lohse M, Usadel B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 2014; 30(15):2114–20. https://doi.org/10.1093/bioinformatics/btu170 PMID: 24695404; PubMed Central PMCID: PMCPMC4103590.
-
(2014)
Bioinformatics
, vol.30
, Issue.15
, pp. 2114-2120
-
-
Bolger, A.M.1
Lohse, M.2
Usadel, B.3
-
33
-
-
67649884743
-
Fast and accurate short read alignment with burrows-wheeler transform
-
PMID: 19451168; PubMed Central PMCID: PMCPMC2705234
-
Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009; 25(14):1754–60. https://doi.org/10.1093/bioinformatics/btp324 PMID: 19451168; PubMed Central PMCID: PMCPMC2705234.
-
(2009)
Bioinformatics
, vol.25
, Issue.14
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
34
-
-
84928987900
-
HTSEQ-A python framework to work with high-throughput sequencing data
-
PMID: 25260700; PubMed Central PMCID: PMCPMC4287950
-
Anders S, Pyl PT, Huber W. HTSeq—a Python framework to work with high-throughput sequencing data. Bioinformatics. 2015; 31(2):166–9. https://doi.org/10.1093/bioinformatics/btu638 PMID: 25260700; PubMed Central PMCID: PMCPMC4287950.
-
(2015)
Bioinformatics
, vol.31
, Issue.2
, pp. 166-169
-
-
Anders, S.1
Pyl, P.T.2
Huber, W.3
-
36
-
-
77955255742
-
Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics
-
PMID: 20454671; PubMed Central PMCID: PMCPMC2862719
-
Fan HC, Quake SR. Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics. PloS one. 2010; 5(5):e10439. https://doi.org/10.1371/journal.pone.0010439 PMID: 20454671; PubMed Central PMCID: PMCPMC2862719.
-
(2010)
Plos One
, vol.5
, Issue.5
, pp. e10439
-
-
Fan, H.C.1
Quake, S.R.2
-
37
-
-
12344259648
-
Analysis of array cgh data: From signal ratio to gain and loss of DNA regions
-
PMID: 15381628
-
Hupe P, Stransky N, Thiery JP, Radvanyi F, Barillot E. Analysis of array CGH data: from signal ratio to gain and loss of DNA regions. Bioinformatics. 2004; 20(18):3413–22. https://doi.org/10.1093/bioinformatics/bth418 PMID: 15381628.
-
(2004)
Bioinformatics
, vol.20
, Issue.18
, pp. 3413-3422
-
-
Hupe, P.1
Stransky, N.2
Thiery, J.P.3
Radvanyi, F.4
Barillot, E.5
-
38
-
-
3543105225
-
Circular binary segmentation for the analysis of array-based DNA copy number data
-
PMID: 15475419
-
Olshen AB, Venkatraman ES, Lucito R, Wigler M. Circular binary segmentation for the analysis of array-based DNA copy number data. Biostatistics. 2004; 5(4):557–72. https://doi.org/10.1093/biostatistics/kxh008 PMID: 15475419.
-
(2004)
Biostatistics
, vol.5
, Issue.4
, pp. 557-572
-
-
Olshen, A.B.1
Venkatraman, E.S.2
Lucito, R.3
Wigler, M.4
-
40
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
PMID: 23128226; PubMed Central PMCID: PMC3498066
-
Genomes Project C, Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, et al. An integrated map of genetic variation from 1,092 human genomes. Nature. 2012; 491(7422):56–65. https://doi.org/10.1038/nature11632 PMID: 23128226; PubMed Central PMCID: PMC3498066.
-
(2012)
Nature
, vol.491
, Issue.7422
, pp. 56-65
-
-
Genomes Project, C.1
Abecasis, G.R.2
Auton, A.3
Brooks, L.D.4
DePristo, M.A.5
Durbin, R.M.6
-
41
-
-
84856050665
-
Sequencing projects bring age-old wisdom to genomics
-
PMID: 22064397
-
Borrell B. Sequencing projects bring age-old wisdom to genomics. Nature medicine. 2011; 17(11):1329. https://doi.org/10.1038/nm1111-1329a PMID: 22064397.
-
(2011)
Nature Medicine
, vol.17
, Issue.11
, pp. 1329
-
-
Borrell, B.1
-
42
-
-
84898743768
-
Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families
-
PMID: 24702956; PubMed Central PMCID: PMC3980410
-
Singleton MV, Guthery SL, Voelkerding KV, Chen K, Kennedy B, Margraf RL, et al. Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families. American journal of human genetics. 2014; 94(4):599–610. https://doi.org/10.1016/j.ajhg.2014.03.010 PMID: 24702956; PubMed Central PMCID: PMC3980410.
-
(2014)
American Journal of Human Genetics
, vol.94
, Issue.4
, pp. 599-610
-
-
Singleton, M.V.1
Guthery, S.L.2
Voelkerding, K.V.3
Chen, K.4
Kennedy, B.5
Margraf, R.L.6
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