Journal of Next Generation Sequencing & Applications

ISSN - 2469-9853

+44 1250400002

Citations Report

Journal of Next Generation Sequencing & Applications : Citations & Metrics Report

Articles published in Journal of Next Generation Sequencing & Applications have been cited by esteemed scholars and scientists all around the world. Journal of Next Generation Sequencing & Applications has got h-index 10, which means every article in Journal of Next Generation Sequencing & Applications has got 10 average citations.

Following are the list of articles that have cited the articles published in Journal of Next Generation Sequencing & Applications.

  2022 2021 2020 2019 2018

Total published articles

0 31 27 0 1

Conference proceedings

0 0 0 0 0

Citations received as per Google Scholar, other indexing platforms and portals

81 96 113 87 65
Journal total citations count 655
Journal impact factor 5.42
Journal 5 years impact factor 7.34
Journal cite score 6.34
Journal h-index 10
Journal Impact Factor 2020 formula
IF= Citations(y)/{Publications(y-1)+ Publications(y-2)} Y= Year
Journal 5-year Impact Factor 2020 formula
Citations(2016 + 2017 + 2018 + 2019 + 2020)/
{Published articles(2016 + 2017 + 2018 + 2019 + 2020)}
Journal citescore
Citescorey = Citationsy + Citationsy-1 + Citationsy-2 + Citations y-3 / Published articlesy + Published articlesy-1 + Published articlesy-2 + Published articles y-3
Important Citations

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.

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.

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.

Canzoniero JV, Park BH. Use of cell free DNA in breast oncology. Biochimica et Biophysica Acta (BBA)-Reviews on Cancer. 2016 Apr 30;1865(2):266-74.

Reid-Bayliss KS, Arron ST, Loeb LA, Bezrookove V, Cleaver JE. Why Cockayne syndrome patients do not get cancer despite their DNA repair deficiency. Proceedings of the National Academy of Sciences. 2016 Sep 6;113(36):10151-6.

Saber A, van der Wekken A, Hiltermann TJ, Kok K, van den Berg A, Groen HJ. Genomic aberrations guiding treatment of non-small cell lung cancer patients. Cancer Treatment Communications. 2015 Dec 31;4:23-33.

Wicke S, Schneeweiss GM. Next-generation organellar genomics: Potentials and pitfalls of high-throughput technologies for molecular evolutionary studies and plant systematics. Next-Generation Sequencing in Plant Systematics. 2015;158.

Gasc C, Peyretaillade E, Peyret P. Sequence capture by hybridization to explore modern and ancient genomic diversity in model and nonmodel organisms. Nucleic acids research. 2016 Jun 2;44(10):4504-18.

Krimmel JD, Schmitt MW, Harrell MI, Agnew KJ, Kennedy SR, Emond MJ, Loeb LA, Swisher EM, Risques RA. Ultra-deep sequencing detects ovarian cancer cells in peritoneal fluid and reveals somatic TP53 mutations in noncancerous tissues. Proceedings of the National Academy of Sciences. 2016 May 24;113(21):6005-10.

Datta S, Budhauliya R, Das B, Chatterjee S. Next-generation sequencing in clinical virology: Discovery of new viruses. World journal of virology. 2015 Aug 12;4(3):265.

Schmitt MW, Loeb LA, Salk JJ. The influence of subclonal resistance mutations on targeted cancer therapy. Nature reviews Clinical oncology. 2016 Jun 1;13(6):335-47.

Schmitt MW, Fox EJ, Prindle MJ, Reid-Bayliss KS, True LD, Radich JP, Loeb LA. Sequencing small genomic targets with high efficiency and extreme accuracy. Nature methods. 2015 May 1;12(5):423-5.

Thakur C. Research & Reviews: Journal of Medical and Health Sciences.

Londhe N, Vyas J. Role of Mitochondrial Genetics in Complex Diseases.

Linderholm A. Ancient DNA: the next generation–chapter and verse. Biological Journal of the Linnean Society. 2016 Jan 1;117(1):150-60.

Garrido-Cardenas JA, Garcia-Maroto F, Alvarez-Bermejo JA, Manzano-Agugliaro F. DNA Sequencing Sensors: An Overview. Sensors. 2017 Mar 14;17(3):588.

Ari Åž, Arikan M. Next-Generation Sequencing: Advantages, Disadvantages, and Future. InPlant Omics: Trends and Applications 2016 (pp. 109-135). Springer International Publishing.

Chang KC, Marton MJ. Past, current and future approaches to querying MAPK pathway activation: status and clinical implications. Personalized Medicine. 2014 Nov;11(8):745-60.

Kim S, Park C, Ji Y, Kim DG, Bae H, van Vrancken M, Kim DH, Kim KM. Deamination Effects in Formalin-Fixed, Paraffin-Embedded Tissue Samples in the Era of Precision Medicine. The Journal of Molecular Diagnostics. 2017 Jan 31;19(1):137-46.

Sultana S. Research and Reviews: Journal of Pharmacy and Pharmaceutical Sciences.

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