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Journal Abstract Search

210 related items for PubMed ID: 26519411

  • 21. RNA-Seq in the Collaborative Cross.
    Green R, Wilkins C, Ferris MT, Gale M.
    Methods Mol Biol; 2017; 1488():251-263. PubMed ID: 27933528
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  • 22. SparkBWA: Speeding Up the Alignment of High-Throughput DNA Sequencing Data.
    Abuín JM, Pichel JC, Pena TF, Amigo J.
    PLoS One; 2016; 11(5):e0155461. PubMed ID: 27182962
    [Abstract] [Full Text] [Related]

  • 23. Bioinformatics: identification of markers from next-generation sequence data.
    Ruperao P, Edwards D.
    Methods Mol Biol; 2015; 1245():29-47. PubMed ID: 25373747
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  • 24. PGen: large-scale genomic variations analysis workflow and browser in SoyKB.
    Liu Y, Khan SM, Wang J, Rynge M, Zhang Y, Zeng S, Chen S, Maldonado Dos Santos JV, Valliyodan B, Calyam PP, Merchant N, Nguyen HT, Xu D, Joshi T.
    BMC Bioinformatics; 2016 Oct 06; 17(Suppl 13):337. PubMed ID: 27766951
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  • 25. Hidden Markov Models in Bioinformatics: SNV Inference from Next Generation Sequence.
    Bian J, Zhou X.
    Methods Mol Biol; 2017 Oct 06; 1552():123-133. PubMed ID: 28224495
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  • 26. Coverage-based consensus calling (CbCC) of short sequence reads and comparison of CbCC results to identify SNPs in chickpea (Cicer arietinum; Fabaceae), a crop species without a reference genome.
    Azam S, Thakur V, Ruperao P, Shah T, Balaji J, Amindala B, Farmer AD, Studholme DJ, May GD, Edwards D, Jones JD, Varshney RK.
    Am J Bot; 2012 Feb 06; 99(2):186-92. PubMed ID: 22301893
    [Abstract] [Full Text] [Related]

  • 27. Do it yourself guide to genome assembly.
    Wajid B, Serpedin E.
    Brief Funct Genomics; 2016 Jan 06; 15(1):1-9. PubMed ID: 25392234
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  • 28. DBG2OLC: Efficient Assembly of Large Genomes Using Long Erroneous Reads of the Third Generation Sequencing Technologies.
    Ye C, Hill CM, Wu S, Ruan J, Ma ZS.
    Sci Rep; 2016 Aug 30; 6():31900. PubMed ID: 27573208
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  • 29. Bioinformatics approaches and resources for single nucleotide polymorphism functional analysis.
    Mooney S.
    Brief Bioinform; 2005 Mar 30; 6(1):44-56. PubMed ID: 15826356
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  • 30. Using Tablet for visual exploration of second-generation sequencing data.
    Milne I, Stephen G, Bayer M, Cock PJ, Pritchard L, Cardle L, Shaw PD, Marshall D.
    Brief Bioinform; 2013 Mar 30; 14(2):193-202. PubMed ID: 22445902
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  • 31. Systematic review of next-generation sequencing simulators: computational tools, features and perspectives.
    Zhao M, Liu D, Qu H.
    Brief Funct Genomics; 2017 May 01; 16(3):121-128. PubMed ID: 27069250
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  • 32. Bioinformatics Data Analysis of Next-Generation Sequencing Data from Heterogeneous Tumor Samples.
    Landman SR, Hwang TH.
    Methods Mol Biol; 2017 May 01; 1633():185-192. PubMed ID: 28735488
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  • 33. ReSeq simulates realistic Illumina high-throughput sequencing data.
    Schmeing S, Robinson MD.
    Genome Biol; 2021 Feb 19; 22(1):67. PubMed ID: 33608040
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  • 34. Evaluation of next-generation sequencing software in mapping and assembly.
    Bao S, Jiang R, Kwan W, Wang B, Ma X, Song YQ.
    J Hum Genet; 2011 Jun 19; 56(6):406-14. PubMed ID: 21525877
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  • 35. NGS for Sequence Variants.
    Teng S.
    Adv Exp Med Biol; 2016 Jun 19; 939():1-20. PubMed ID: 27807741
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  • 36. Haplotag: Software for Haplotype-Based Genotyping-by-Sequencing Analysis.
    Tinker NA, Bekele WA, Hattori J.
    G3 (Bethesda); 2016 Apr 07; 6(4):857-63. PubMed ID: 26818073
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  • 37. Tablet--next generation sequence assembly visualization.
    Milne I, Bayer M, Cardle L, Shaw P, Stephen G, Wright F, Marshall D.
    Bioinformatics; 2010 Feb 01; 26(3):401-2. PubMed ID: 19965881
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  • 38. Challenges in exome analysis by LifeScope and its alternative computational pipelines.
    Pranckevičiene E, Rančelis T, Pranculis A, Kučinskas V.
    BMC Res Notes; 2015 Sep 07; 8():421. PubMed ID: 26346699
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  • 39. mod_bio: Apache modules for Next-Generation sequencing data.
    Lindenbaum P, Redon R.
    Bioinformatics; 2015 Jan 01; 31(1):112-3. PubMed ID: 25192739
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  • 40. An investigation of causes of false positive single nucleotide polymorphisms using simulated reads from a small eukaryote genome.
    Ribeiro A, Golicz A, Hackett CA, Milne I, Stephen G, Marshall D, Flavell AJ, Bayer M.
    BMC Bioinformatics; 2015 Nov 11; 16():382. PubMed ID: 26558718
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