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For: Bahassi el M, Stambrook PJ. Next-generation sequencing technologies: breaking the sound barrier of human genetics. Mutagenesis 2014;29:303-10. [PMID: 25150023 DOI: 10.1093/mutage/geu031] [Cited by in Crossref: 81] [Cited by in F6Publishing: 84] [Article Influence: 10.1] [Reference Citation Analysis]
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6 D. Magar N, Shah P, Harish K, C. Bosamia T, M. Barbadikar K, M. Shukla Y, Phule A, N. Zala H, Sheshu Madhav M, Kumar Mangrauthia S, Naga Neeraja C, Meenakshi Sundaram R. Gene Expression and Transcriptome Sequencing: Basics, Analysis, Advances. Gene Expression [Working Title] 2022. [DOI: 10.5772/intechopen.105929] [Reference Citation Analysis]
7 Cheng D, Huang S, Chin W, Hung S, Tsai H, Chu JJH, Chao C, Wang J. Impact of Intrahost NS5 Nucleotide Variations on Dengue Virus Replication. Front Microbiol 2022;13:894200. [DOI: 10.3389/fmicb.2022.894200] [Reference Citation Analysis]
8 Huang Y, Fang T, Kung B, Chen C. Two Genetic Mechanisms in Two Siblings with Intellectual Disability, Autism Spectrum Disorder, and Psychosis. JPM 2022;12:1013. [DOI: 10.3390/jpm12061013] [Reference Citation Analysis]
9 Almes M, Spraul A, Ruiz M, Girard M, Roquelaure B, Laborde N, Gottrand F, Turquet A, Lamireau T, Dabadie A, Bonneton M, Thebaut A, Rohmer B, Lacaille F, Broué P, Fabre A, Mention-mulliez K, Bouligand J, Jacquemin E, Gonzales E. Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis. Diagnostics 2022;12:1169. [DOI: 10.3390/diagnostics12051169] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Alves F, Martins FMS, Areias M, Muñoz-Mérida A. Automating microsatellite screening and primer design from multi-individual libraries using Micro-Primers. Sci Rep 2022;12:295. [PMID: 34997147 DOI: 10.1038/s41598-021-04275-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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12 Openshaw MR, McVeigh TP. Non-invasive Technology Advances in Cancer-A Review of the Advances in the Liquid Biopsy for Endometrial and Ovarian Cancers. Front Digit Health 2020;2:573010. [PMID: 34713045 DOI: 10.3389/fdgth.2020.573010] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
13 Smedley MA, Hayta S, Clarke M, Harwood WA. CRISPR-Cas9 Based Genome Editing in Wheat. Curr Protoc 2021;1:e65. [PMID: 33687760 DOI: 10.1002/cpz1.65] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
14 Hu T, Chitnis N, Monos D, Dinh A. Next-generation sequencing technologies: An overview. Hum Immunol 2021:S0198-8859(21)00062-8. [PMID: 33745759 DOI: 10.1016/j.humimm.2021.02.012] [Cited by in Crossref: 63] [Cited by in F6Publishing: 76] [Article Influence: 31.5] [Reference Citation Analysis]
15 Liu W, Wu Q. Analysis method and algorithm design of biological sequence problem based on generalized k-mer vector. Appl Math J Chin Univ 2021;36:114-127. [DOI: 10.1007/s11766-021-4033-x] [Reference Citation Analysis]
16 Leung JY, Chia K, Ong DST, Taneja R. Interweaving Tumor Heterogeneity into the Cancer Epigenetic/Metabolic Axis. Antioxid Redox Signal 2020;33:946-65. [PMID: 31841357 DOI: 10.1089/ars.2019.7942] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
17 Mikhaylenko DS, Tanas AS, Zaletaev DV, Nemtsova MV. Application Areas of Traditional Molecular Genetic Methods and NGS in relation to Hereditary Urological Cancer Diagnosis. J Oncol 2020;2020:7363102. [PMID: 32612654 DOI: 10.1155/2020/7363102] [Reference Citation Analysis]
18 Shigeto H, Yamada E, Kitamatsu M, Ohtsuki T, Iizuka A, Akiyama Y, Yamamura S. Analysis of Single Nucleotide-Mutated Single-Cancer Cells Using the Combined Technologies of Single-Cell Microarray Chips and Peptide Nucleic Acid-DNA Probes. Micromachines (Basel) 2020;11:E628. [PMID: 32605095 DOI: 10.3390/mi11070628] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
19 Madhura MG, Rao RS, Patil S, Fageeh HN, Alhazmi A, Awan KH. Advanced diagnostic aids for oral cancer. Dis Mon 2020;66:101034. [PMID: 32594996 DOI: 10.1016/j.disamonth.2020.101034] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
20 Papa R, Rusmini M, Volpi S, Caorsi R, Picco P, Grossi A, Caroli F, Bovis F, Musso V, Obici L, Castana C, Ravelli A, Van Gijn ME, Ceccherini I, Gattorno M. Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers. Rheumatology (Oxford) 2020;59:344-60. [PMID: 31325311 DOI: 10.1093/rheumatology/kez270] [Cited by in Crossref: 21] [Cited by in F6Publishing: 23] [Article Influence: 7.0] [Reference Citation Analysis]
21 Arslan AB, Zamani AG, Pekcan S, Yıldırım MS. A Novel Pathogenic Variant of the CFTR Gene in a Patient with Cystic Fibrosis Phenotype-c.4096A > T. J Pediatr Genet 2020;9:40-3. [PMID: 31976142 DOI: 10.1055/s-0039-1694964] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
22 Song J, Hussaini M. Adopting solutions for annotation and reporting of next generation sequencing in clinical practice. Pract Lab Med 2020;19:e00154. [PMID: 32099889 DOI: 10.1016/j.plabm.2020.e00154] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
23 Weng J, Li DD, Jiang BG, Yin XF. Temporal changes in the spinal cord transcriptome after peripheral nerve injury. Neural Regen Res 2020;15:1360-7. [PMID: 31960825 DOI: 10.4103/1673-5374.272618] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
24 Yadav V, Satheesh Kumar T. Present scenario of antibiotic use in veterinary practice: importance of wastewater microbiology. Current Developments in Biotechnology and Bioengineering 2020. [DOI: 10.1016/b978-0-12-819722-6.00009-2] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
25 Robles Montoya RI, Valenzuela Ruiz V, Parra Cota FI, Santoyo G, de los Santos-villalobos S. Description of a Polyphasic Taxonomic Approach for Plant Growth-Promoting Rhizobacteria (PGPR). Microbial Services in Restoration Ecology 2020. [DOI: 10.1016/b978-0-12-819978-7.00017-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
26 Lin Y, Li X, Huang X, Zheng D, Liu Y, Lan F, Wang Z. Hybrid minigene splicing assay verifies the pathogenicity of a novel splice site variant in the COL1A1 gene of a chinese patient with osteogenesis imperfecta type I. Injury 2019;50:2215-9. [PMID: 31653500 DOI: 10.1016/j.injury.2019.10.033] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
27 Venugopal N, Yeh J, Kodeboyina SK, Lee TJ, Sharma S, Patel N, Sharma A. Differences in the early stage gene expression profiles of lung adenocarcinoma and lung squamous cell carcinoma. Oncol Lett 2019;18:6572-82. [PMID: 31788115 DOI: 10.3892/ol.2019.11013] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
28 Sas V, Moisoiu V, Teodorescu P, Tranca S, Pop L, Iluta S, Pasca S, Blag C, Man S, Roman A, Constantinescu C, Rus I, Buse M, Fetica B, Marian M, Selicean C, Berindan-Neagoe I, Petrushev B, Bumbea H, Tanase A, Zdrenghea M, Fuji S, Kitano S, Tomuleasa C; Romanian-Japanese Working Group of the Romanian Society for Bone Marrow Transplantation. Approach to the Adult Acute Lymphoblastic Leukemia Patient. J Clin Med 2019;8:E1175. [PMID: 31390838 DOI: 10.3390/jcm8081175] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 2.5] [Reference Citation Analysis]
29 Hamdan D, Nguyen TT, Leboeuf C, Meles S, Janin A, Bousquet G. Genomics applied to the treatment of breast cancer. Oncotarget 2019;10:4786-801. [PMID: 31413819 DOI: 10.18632/oncotarget.27102] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 3.5] [Reference Citation Analysis]
30 Wang H, Hart DJ, An Y. Functional Metagenomic Technologies for the Discovery of Novel Enzymes for Biomass Degradation and Biofuel Production. Bioenerg Res 2019;12:457-70. [DOI: 10.1007/s12155-019-10005-w] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
31 Salis C, Papakonstantinou E, Pierouli K, Mitsis A, Basdeki L, Megalooikonomou V, Vlachakis D, Hagidimitriou M. A genomic data mining pipeline for 15 species of the genus Olea. EMBnet J 2019;24:e922. [PMID: 31218210 DOI: 10.14806/ej.24.0.922] [Reference Citation Analysis]
32 Fasullo M. Cellular Responses to Aflatoxin-Associated DNA Adducts. DNA Repair- An Update 2019. [DOI: 10.5772/intechopen.81763] [Reference Citation Analysis]
33 Smith CP, Czarniecki M, Mehralivand S, Stoyanova R, Choyke PL, Harmon S, Turkbey B. Radiomics and radiogenomics of prostate cancer. Abdom Radiol (NY) 2019;44:2021-9. [PMID: 29926137 DOI: 10.1007/s00261-018-1660-7] [Cited by in Crossref: 27] [Cited by in F6Publishing: 24] [Article Influence: 6.8] [Reference Citation Analysis]
34 Hsieh PC, Wang CC, Tsai CL, Yeh YM, Lee YS, Wu YR. POLG R964C and GBA L444P mutations in familial Parkinson's disease: Case report and literature review. Brain Behav 2019;9:e01281. [PMID: 30941926 DOI: 10.1002/brb3.1281] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
35 Wang B, Kumar V, Olson A, Ware D. Reviving the Transcriptome Studies: An Insight Into the Emergence of Single-Molecule Transcriptome Sequencing. Front Genet 2019;10:384. [PMID: 31105749 DOI: 10.3389/fgene.2019.00384] [Cited by in Crossref: 58] [Cited by in F6Publishing: 61] [Article Influence: 14.5] [Reference Citation Analysis]
36 Fischer J, Walker LC, Robinson BA, Frizelle FA, Church JM, Eglinton TW. Clinical implications of the genetics of sporadic colorectal cancer. ANZ J Surg 2019;89:1224-9. [PMID: 30919552 DOI: 10.1111/ans.15074] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 3.3] [Reference Citation Analysis]
37 Yan R, Schnabel KE, Guo X, Gardner JPA. Development and characterization of 20 polymorphic microsatellite loci in the deep sea squat lobster, Munida isos Ahyong and Poore, 2004 and cross-amplification in two congeneric species. J Genet 2019;98. [DOI: 10.1007/s12041-019-1062-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
38 Chen HL, Li HY, Wu JF, Wu SH, Chen HL, Yang YH, Hsu YH, Liou BY, Chang MH, Ni YH. Panel-Based Next-Generation Sequencing for the Diagnosis of Cholestatic Genetic Liver Diseases: Clinical Utility and Challenges. J Pediatr 2019;205:153-159.e6. [PMID: 30366773 DOI: 10.1016/j.jpeds.2018.09.028] [Cited by in Crossref: 31] [Cited by in F6Publishing: 30] [Article Influence: 7.8] [Reference Citation Analysis]
39 Yada T. Genome Alignment. Encyclopedia of Bioinformatics and Computational Biology 2019. [DOI: 10.1016/b978-0-12-809633-8.20237-9] [Reference Citation Analysis]
40 Gupta N, Verma VK. Next-Generation Sequencing and Its Application: Empowering in Public Health Beyond Reality. Microorganisms for Sustainability 2019. [DOI: 10.1007/978-981-13-8844-6_15] [Cited by in Crossref: 7] [Article Influence: 1.8] [Reference Citation Analysis]
41 Eguchi H, Okazaki Y. Next-Generation Sequencing for Genetic Diagnosis of Hereditary Colorectal Cancer and Polyposis Syndrome. Recent Advances in the Treatment of Colorectal Cancer 2019. [DOI: 10.1007/978-981-13-3050-6_10] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
42 Kanno R, Tanaka D, Nanamiya H, Isogai T. ReALLEN: structural variation discovery in cancer genome by sensitive analysis of single-end reads.. [DOI: 10.1101/506329] [Reference Citation Analysis]
43 Bagnasco SM. Beyond the microscope: interpreting renal biopsy findings in the era of precision medicine. Am J Physiol Renal Physiol 2018;315:F1652-5. [PMID: 30280602 DOI: 10.1152/ajprenal.00407.2018] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
44 Sapna G, Gokul S. Next generation sequencing in oral disease diagnostics. World J Stomatol 2018; 6(2): 6-10 [DOI: 10.5321/wjs.v6.i2.6] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
45 Hamdan D, Nguyen TT, Dao VT, Bouchtaoui ME, Janin A, Bousquet G. Génomique du cancer du sein appliquée aux traitements. Revue Francophone des Laboratoires 2018;2018:52-60. [DOI: 10.1016/s1773-035x(18)30323-x] [Reference Citation Analysis]
46 Ghorbani Mojarrad N, Williams C, Guggenheim JA. A genetic risk score and number of myopic parents independently predict myopia. Ophthalmic Physiol Opt 2018;38:492-502. [PMID: 30182516 DOI: 10.1111/opo.12579] [Cited by in Crossref: 18] [Cited by in F6Publishing: 25] [Article Influence: 3.6] [Reference Citation Analysis]
47 Ganesh P, Gupta G, Saini S, Paul K. Nucl2Vec : Local alignment of DNA sequences using Distributed Vector Representation.. [DOI: 10.1101/401851] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
48 Barros-Silva D, Marques CJ, Henrique R, Jerónimo C. Profiling DNA Methylation Based on Next-Generation Sequencing Approaches: New Insights and Clinical Applications. Genes (Basel) 2018;9:E429. [PMID: 30142958 DOI: 10.3390/genes9090429] [Cited by in Crossref: 76] [Cited by in F6Publishing: 77] [Article Influence: 15.2] [Reference Citation Analysis]
49 Lian Y, Chen L, Meng L, Zhang Q. Construction of the network of critical paths on Blood-stasis syndrome of hypertension based on mRNA sequencing. European Journal of Integrative Medicine 2018;20:73-78. [DOI: 10.1016/j.eujim.2018.04.004] [Reference Citation Analysis]
50 Chen J, Li X, Niu Y, Wu Z, Qiu G. Functional and In Silico Assessment of GDF3 Gene Variants in a Chinese Congenital Scoliosis Population. Med Sci Monit 2018;24:2992-3001. [PMID: 29735971 DOI: 10.12659/MSM.910232] [Reference Citation Analysis]
51 Oakeson KF, Wagner JM, Mendenhall M, Rohrwasser A, Atkinson-Dunn R. Bioinformatic Analyses of Whole-Genome Sequence Data in a Public Health Laboratory. Emerg Infect Dis 2017;23:1441-5. [PMID: 28820135 DOI: 10.3201/eid2309.170416] [Cited by in Crossref: 31] [Cited by in F6Publishing: 31] [Article Influence: 6.2] [Reference Citation Analysis]
52 Yudin NS, Barkhash AV, Maksimov VN, Ignatieva EV, Romaschenko AG. Human Genetic Predisposition to Diseases Caused by Viruses from Flaviviridae Family. Mol Biol 2018;52:165-81. [DOI: 10.1134/s0026893317050223] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.8] [Reference Citation Analysis]
53 Tomita M, Ishii K. Genetic Performance of the Semidwarfing Allele sd1 Derived from a Japonica Rice Cultivar and Minimum Requirements to Detect Its Single-Nucleotide Polymorphism by MiSeq Whole-Genome Sequencing. Biomed Res Int 2018;2018:4241725. [PMID: 29850513 DOI: 10.1155/2018/4241725] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 2.2] [Reference Citation Analysis]
54 Hirsch FR, Kerr KM, Bunn PA Jr, Kim ES, Obasaju C, Pérol M, Bonomi P, Bradley JD, Gandara D, Jett JR, Langer CJ, Natale RB, Novello S, Paz-Ares L, Ramalingam SS, Reck M, Reynolds CH, Smit EF, Socinski MA, Spigel DR, Stinchcombe TE, Vansteenkiste JF, Wakelee H, Thatcher N. Molecular and Immune Biomarker Testing in Squamous-Cell Lung Cancer: Effect of Current and Future Therapies and Technologies. Clin Lung Cancer 2018;19:331-9. [PMID: 29773328 DOI: 10.1016/j.cllc.2018.03.014] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 2.2] [Reference Citation Analysis]
55 Prasongkit J, de Freitas Martins E, de Souza FAL, Scopel WL, Amorim RG, Amornkitbamrung V, Rocha AR, Scheicher RH. Topological Line Defects Around Graphene Nanopores for DNA Sequencing. J Phys Chem C 2018;122:7094-9. [DOI: 10.1021/acs.jpcc.8b00241] [Cited by in Crossref: 19] [Cited by in F6Publishing: 20] [Article Influence: 3.8] [Reference Citation Analysis]
56 Nguyen HH, Park J, Park SJ, Lee CS, Hwang S, Shin YB, Ha TH, Kim M. Long-Term Stability and Integrity of Plasmid-Based DNA Data Storage. Polymers (Basel) 2018;10:E28. [PMID: 30966073 DOI: 10.3390/polym10010028] [Cited by in Crossref: 20] [Cited by in F6Publishing: 22] [Article Influence: 4.0] [Reference Citation Analysis]
57 Zhang B, Zhang G, Ji W, Yang R, Zou G, Chen K, Wei K, Gardner JPA. Development and characterization of 32 SNP markers for the northern snakehead (Channa argus) using high resolution melting (HRM). Conservation Genet Resour 2017;9:631-634. [DOI: 10.1007/s12686-017-0743-z] [Reference Citation Analysis]
58 Chang YS, Huang HD, Yeh KT, Chang JG. Evaluation of whole exome sequencing by targeted gene sequencing and Sanger sequencing. Clin Chim Acta 2017;471:222-32. [PMID: 28624499 DOI: 10.1016/j.cca.2017.06.015] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
59 Zhao S, Watrous K, Zhang C, Zhang B. Cloud Computing for Next-Generation Sequencing Data Analysis. Cloud Computing - Architecture and Applications 2017. [DOI: 10.5772/66732] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.2] [Reference Citation Analysis]
60 Incoronato M, Aiello M, Infante T, Cavaliere C, Grimaldi AM, Mirabelli P, Monti S, Salvatore M. Radiogenomic Analysis of Oncological Data: A Technical Survey. Int J Mol Sci 2017;18:E805. [PMID: 28417933 DOI: 10.3390/ijms18040805] [Cited by in Crossref: 74] [Cited by in F6Publishing: 79] [Article Influence: 12.3] [Reference Citation Analysis]
61 Teng L, Deng W, Lu J, Zhang J, Ren X, Duan H, Chuai S, Duan F, Gao W, Lu T, Wu H, Liang Z. Hobnail variant of papillary thyroid carcinoma: molecular profiling and comparison to classical papillary thyroid carcinoma, poorly differentiated thyroid carcinoma and anaplastic thyroid carcinoma. Oncotarget 2017;8:22023-33. [PMID: 28423545 DOI: 10.18632/oncotarget.15786] [Cited by in Crossref: 37] [Cited by in F6Publishing: 39] [Article Influence: 6.2] [Reference Citation Analysis]
62 van der Merwe N, Peeters AV, Pienaar FM, Bezuidenhout J, van Rensburg SJ, Kotze MJ. Exome Sequencing in a Family with Luminal-Type Breast Cancer Underpinned by Variation in the Methylation Pathway. Int J Mol Sci 2017;18:E467. [PMID: 28241424 DOI: 10.3390/ijms18020467] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 1.5] [Reference Citation Analysis]
63 Tsakogiannis D, Gartzonika C, Levidiotou-Stefanou S, Markoulatos P. Molecular approaches for HPV genotyping and HPV-DNA physical status. Expert Rev Mol Med 2017;19:e1. [PMID: 28162121 DOI: 10.1017/erm.2017.2] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 5.3] [Reference Citation Analysis]
64 Li L, Jin M, Sun C, Wang X, Xie S, Zhou G, van den Berg A, Eijkel JC, Shui L. High Efficiency Hydrodynamic DNA Fragmentation in a Bubbling System. Sci Rep 2017;7:40745. [PMID: 28098208 DOI: 10.1038/srep40745] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
65 Toh H, Shirane K, Miura F, Kubo N, Ichiyanagi K, Hayashi K, Saitou M, Suyama M, Ito T, Sasaki H. Software updates in the Illumina HiSeq platform affect whole-genome bisulfite sequencing. BMC Genomics 2017;18:31. [PMID: 28056787 DOI: 10.1186/s12864-016-3392-9] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 3.7] [Reference Citation Analysis]
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67 Gillet NA, Melamed A, Bangham CRM. High-Throughput Mapping and Clonal Quantification of Retroviral Integration Sites. Methods in Molecular Biology 2017. [DOI: 10.1007/978-1-4939-6872-5_10] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
68 Carapito R, Radosavljevic M, Bahram S. Next-Generation Sequencing of the HLA locus: Methods and impacts on HLA typing, population genetics and disease association studies. Human Immunology 2016;77:1016-23. [DOI: 10.1016/j.humimm.2016.04.002] [Cited by in Crossref: 55] [Cited by in F6Publishing: 49] [Article Influence: 7.9] [Reference Citation Analysis]
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