alexa Citations Report - Journal of Next Generation Sequencing and Applic
ISSN 2469-9853

Journal of Next Generation Sequencing & Applications
Open Access

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The articles published in Journal of Next Generation Sequencing & Applications have been cited 53 times by eminent researchers all around the world. Following is the list of articles that have cited the articles published in Journal of Next Generation Sequencing & Applications.

 
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Ståhlberg A, Krzyzanowski PM, Egyud M, Filges S, Stein L, Godfrey TE. Simple multiplexed PCR-based barcoding of DNA for ultrasensitive mutation detection by next-generation sequencing. Nature Protocols. 2017 Apr 1;12(4):664-82.

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Zhang Y, Cao L, Nguyen D, Lu H. TP53 mutations in epithelial ovarian cancer. Translational Cancer Research. 2016 Sep 19;5(6):650-63.

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Ju F, Fang HH, Zhang T. Application of Metagenomics in Environmental Anaerobic Technology. InAnaerobic Biotechnology: Environmental Protection and Resource Recovery 2015 Aug 24 (pp. 73-108). Imperial College Press.

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Ju F, 鞠峰. Linking microbial communities, environmental factors and performance of biological treatment reactors using metagenomics. HKU Theses Online (HKUTO). 2015.

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Holzer FS, Mastroleo I, Mertelsmann R, Mollerach AF. The iterative informed consent model for the feedback of incidental findings in human health research using WGS procedures El modelo iterativo de consentimiento informado para hallazgos incidentales en la investigación clínica con secuenciación genómica completa.

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Oldrati V, Arrell M, Violette A, Perret F, Sprüngli X, Wolfender JL, Stöcklin R. Advances in venomics. Molecular BioSystems. 2016;12(12):3530-43.

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Akogwu I, Wang N, Zhang C, Choi H, Hong H, Gong P. Factorial analysis of error correction performance using simulated next-generation sequencing data. InBioinformatics and Biomedicine (BIBM), 2016 IEEE International Conference on 2016 Dec 15 (pp. 1164-1169). IEEE.

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Lefevre E, Cooper E, Stapleton HM, Gunsch CK. Characterization and Adaptation of Anaerobic Sludge Microbial Communities Exposed to Tetrabromobisphenol A. PloS one. 2016 Jul 27;11(7):e0157622.

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Li N, Wang X, Liu Z. Next-Generation Sequencing Technologies and the Assembly of Short Reads into Reference Genome Sequences. Bioinformatics in Aquaculture. 2017 Apr 24.

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Sugawara R, Yamada S, Tu Z, Sugawara A, Suzuki K, Hoshiba T, Eisaka S, Yamaguchi A. Rapid and reliable species identification of wild mushrooms by matrix assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS). Analytica Chimica Acta. 2016 Aug 31;934:163-9.

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Ye W, Chen Y, Zhang Y, Xu Y. H-BLAST: a fast protein sequence alignment toolkit on heterogeneous computers with GPUs. Bioinformatics (Oxford, England). 2017 Jan 13.

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Holzer F. The iterative informed consent model for the feedback of incidental findings in human health research using WGS procedures. Genetic Counselling.;2(4).

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Jefferies MT. Evaluating synergy between deregulation of the Wnt, PI3-Kinase and MAP-Kinase pathways in prostate tumourigenesis (Doctoral dissertation, Cardiff University).

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Ahn EH, Lee SH, Kim JY, Chang CC, Loeb LA. Decreased mitochondrial mutagenesis during transformation of human breast stem cells into tumorigenic cells. Cancer research. 2016 Aug 1;76(15):4569-78.

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Ahn EH, Hirohata K, Kohrn BF, Fox EJ, Chang CC, Loeb LA. Detection of ultra-rare mitochondrial mutations in breast stem cells by Duplex Sequencing. PloS one. 2015 Aug 25;10(8):e0136216.

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Lynch T, Petkau A, Knox N, Graham M, Van Domselaar G. A Primer on Infectious Disease Bacterial Genomics. Clinical Microbiology Reviews. 2016 Oct 1;29(4):881-913.

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Trémeaux P, Caporossi A, Thélu MA, Blum M, Leroy V, Morand P, Larrat S. Hepatitis C virus whole genome sequencing: current methods/issues and future challenges. Critical reviews in clinical laboratory sciences. 2016 Sep 2;53(5):341-51.

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Melo AT, Bartaula R, Hale I. GBS-SNP-CROP: a reference-optional pipeline for SNP discovery and plant germplasm characterization using variable length, paired-end genotyping-by-sequencing data. BMC bioinformatics. 2016 Jan 12;17(1):29.

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Ståhlberg A, Krzyzanowski PM, Jackson JB, Egyud M, Stein L, Godfrey TE. Simple, multiplexed, PCR-based barcoding of DNA enables sensitive mutation detection in liquid biopsies using sequencing. Nucleic acids research. 2016 Apr 7:gkw224.

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Haque MM, Bose T, Dutta A, Reddy CV, Mande SS. CS-SCORE: Rapid identification and removal of human genome contaminants from metagenomic datasets. Genomics. 2015 Aug 31;106(2):116-21.

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