Results 181 to 190 of about 6,043 (204)

Scalable and efficient DNA sequencing analysis on different compute infrastructures aiding variant discovery. [PDF]

NAR Genom Bioinform
Hanssen F, Garcia MU, Folkersen L, Pedersen AS, Lescai F, Jodoin S, Miller E, Seybold M, Wacker O, Smith N, Gabernet G, Nahnsen S.   +11 more
europepmc   +1 more source

Quantitative functional profiling of ERCC2 mutations deciphers cisplatin sensitivity in bladder cancer. [PDF]

J Clin Invest
Börcsök J, Gopaul D, Devesa-Serrano D, Mooser C, Jonsson N, Cagiada M, Stormoen DR, Ataya MN, Guercio BJ, Kaimakliotis HZ, Iyer G, Lindorff-Larsen K, Dyrskjøt L, Mouw KW, Szallasi Z, Sørensen CS.   +15 more
europepmc   +1 more source

HRProfiler Detects Homologous Recombination Deficiency in Breast and Ovarian Cancers Using Whole-Genome and Whole-Exome Sequencing Data. [PDF]

Cancer Res
Abbasi A, Steele CD, Bergstrom EN, Khandekar A, Farswan A, McKay RR, Pillay N, Alexandrov LB.   +7 more
europepmc   +1 more source

Comprehensive genomic and transcriptomic analyses reveal prognostic stratification for esophageal squamous cell carcinoma. [PDF]

Signal Transduct Target Ther
Gao J, Wang Q, Fu F, Zhao Y, Yang T, Li X, Sun Y, Hu H, Ma L, Miao L, Luo X, Ye T, Zhang Y, Zhang Y, Huang Z, Li H, Shao L, Xu M, Zhao K, Zhang S, Zhang M, Wang J, Dai C, Shang X, An T, Zhang Y, Xiang J, Cao Z, Li B, Chen H.   +29 more
europepmc   +1 more source

Annual Sickle Cell & Thalassaemia Conference (ASCAT) ‐ October 2023

HemaSphere
openaire   +1 more source

Annual Sickle Cell & Thalassaemia Conference (ASCAT) ‐ October 2024

HemaSphere
openaire   +1 more source

Detecting HRD in whole-genome and whole-exome sequenced breast and ovarian cancers

Abbasi A, Steele CD, Bergstrom EN, Khandekar A, Farswan A, Mckay RR, Pillay N, Alexandrov LB.   +7 more
europepmc   +1 more source

Pervasive Chromosomal Instability Drives the Karyotypic Evolution of Hypodiploid Tumours

Loughran E, McLysaght A, Ní Leathlobhair M.   +2 more
europepmc   +1 more source

Activation of Wnt/β-catenin signalling by mutually exclusiveFBXW11andCTNNB1hotspot mutations drives salivary gland basal cell adenoma

Wong K, Bishop JA, Weinreb I, Motta M, Del Castillo Velasco-Herrera M, Bellacchio E, Ferreira I, van der Weyden L, Boccacino JM, Rotundo G, Ciolfi A, Cheema S, Olvera-León R, Offord V, Droop A, Vermes I, Allgaeuer M, Hyrcza M, Anderson E, Smith K, de Saint Aubain N, Mogler C, Stenzinger A, Arends MJ, Brenn T, Tartaglia M, Adams DJ.   +26 more
europepmc   +1 more source