BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 25399029)

  • 21. Refined repetitive sequence searches utilizing a fast hash function and cross species information retrievals.
    Reneker J; Shyu CR
    BMC Bioinformatics; 2005 May; 6():111. PubMed ID: 15869708
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Multiple organism algorithm for finding ultraconserved elements.
    Christley S; Lobo NF; Madey G
    BMC Bioinformatics; 2008 Jan; 9():15. PubMed ID: 18186941
    [TBL] [Abstract][Full Text] [Related]  

  • 23. LTRharvest, an efficient and flexible software for de novo detection of LTR retrotransposons.
    Ellinghaus D; Kurtz S; Willhoeft U
    BMC Bioinformatics; 2008 Jan; 9():18. PubMed ID: 18194517
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fast detection of maximal exact matches via fixed sampling of query K-mers and Bloom filtering of index K-mers.
    Liu Y; Zhang LY; Li J
    Bioinformatics; 2019 Nov; 35(22):4560-4567. PubMed ID: 30994891
    [TBL] [Abstract][Full Text] [Related]  

  • 25. MUMmer4: A fast and versatile genome alignment system.
    Marçais G; Delcher AL; Phillippy AM; Coston R; Salzberg SL; Zimin A
    PLoS Comput Biol; 2018 Jan; 14(1):e1005944. PubMed ID: 29373581
    [TBL] [Abstract][Full Text] [Related]  

  • 26. PRIMEX: rapid identification of oligonucleotide matches in whole genomes.
    Lexa M; Valle G
    Bioinformatics; 2003 Dec; 19(18):2486-8. PubMed ID: 14668240
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Accurate multiple alignment of distantly related genome sequences using filtered spaced word matches as anchor points.
    Leimeister CA; Dencker T; Morgenstern B
    Bioinformatics; 2019 Jan; 35(2):211-218. PubMed ID: 29992260
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Efficient computation of absent words in genomic sequences.
    Herold J; Kurtz S; Giegerich R
    BMC Bioinformatics; 2008 Mar; 9():167. PubMed ID: 18366790
    [TBL] [Abstract][Full Text] [Related]  

  • 29. MICA: A fast short-read aligner that takes full advantage of Many Integrated Core Architecture (MIC).
    Luo R; Cheung J; Wu E; Wang H; Chan SH; Law WC; He G; Yu C; Liu CM; Zhou D; Li Y; Li R; Wang J; Zhu X; Peng S; Lam TW
    BMC Bioinformatics; 2015; 16 Suppl 7(Suppl 7):S10. PubMed ID: 25952019
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Informational and linguistic analysis of large genomic sequence collections via efficient Hadoop cluster algorithms.
    Ferraro Petrillo U; Roscigno G; Cattaneo G; Giancarlo R
    Bioinformatics; 2018 Jun; 34(11):1826-1833. PubMed ID: 29342232
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Long Fragment Aligner called ALFALFA.
    Vyverman M; Baets BD; Fack V; Dawyndt P
    BMC Bioinformatics; 2015 May; 16(1):159. PubMed ID: 25971785
    [TBL] [Abstract][Full Text] [Related]  

  • 32. BWA-MEME: BWA-MEM emulated with a machine learning approach.
    Jung Y; Han D
    Bioinformatics; 2022 Apr; 38(9):2404-2413. PubMed ID: 35253835
    [TBL] [Abstract][Full Text] [Related]  

  • 33. RACER: Rapid and accurate correction of errors in reads.
    Ilie L; Molnar M
    Bioinformatics; 2013 Oct; 29(19):2490-3. PubMed ID: 23853064
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fast index based algorithms and software for matching position specific scoring matrices.
    Beckstette M; Homann R; Giegerich R; Kurtz S
    BMC Bioinformatics; 2006 Aug; 7():389. PubMed ID: 16930469
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel definition and algorithm for chaining fragments with proportional overlaps.
    Uricaru R; Mancheron A; Rivals E
    J Comput Biol; 2011 Sep; 18(9):1141-54. PubMed ID: 21899421
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Efficient merging of genome profile alignments.
    Hennig A; Nieselt K
    Bioinformatics; 2019 Jul; 35(14):i71-i80. PubMed ID: 31510683
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Murasaki: a fast, parallelizable algorithm to find anchors from multiple genomes.
    Popendorf K; Tsuyoshi H; Osana Y; Sakakibara Y
    PLoS One; 2010 Sep; 5(9):e12651. PubMed ID: 20885980
    [TBL] [Abstract][Full Text] [Related]  

  • 38. GeCo++: a C++ library for genomic features computation and annotation in the presence of variants.
    Cereda M; Sironi M; Cavalleri M; Pozzoli U
    Bioinformatics; 2011 May; 27(9):1313-5. PubMed ID: 21398667
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Rapid and sensitive dot-matrix methods for genome analysis.
    Huang Y; Zhang L
    Bioinformatics; 2004 Mar; 20(4):460-6. PubMed ID: 14764561
    [TBL] [Abstract][Full Text] [Related]  

  • 40. SA-SSR: a suffix array-based algorithm for exhaustive and efficient SSR discovery in large genetic sequences.
    Pickett BD; Karlinsey SM; Penrod CE; Cormier MJ; Ebbert MT; Shiozawa DK; Whipple CJ; Ridge PG
    Bioinformatics; 2016 Sep; 32(17):2707-9. PubMed ID: 27170037
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.