Publications

Found 6 results
Author Title Type [ Year(Asc)]
Filters: Keyword is High-Throughput Nucleotide Sequencing  [Clear All Filters]
2024
Meleshko D, Prjbelski AD, Raiko M, Tomescu AI, Tilgner H, Hajirasouliha I.  2024.  cloudrnaSPAdes: isoform assembly using bulk barcoded RNA sequencing data.. Bioinformatics. 40(2)
Gong B, Li D, Łabaj PP, Pan B, Novoradovskaya N, Thierry-Mieg D, Thierry-Mieg J, Chen G, Lucas ABergstrom, LoCoco JS et al..  2024.  Targeted DNA-seq and RNA-seq of Reference Samples with Short-read and Long-read Sequencing.. Sci Data. 11(1):892.
2023
Foord C, Hsu J, Jarroux J, Hu W, Belchikov N, Pollard S, He Y, Joglekar A, Tilgner HU.  2023.  The variables on RNA molecules: concert or cacophony? Answers in long-read sequencing. Nat Methods. 20(1):20-24.
2022
Mikheenko A, Prjibelski AD, Joglekar A, Tilgner HU.  2022.  Sequencing of individual barcoded cDNAs using Pacific Biosciences and Oxford Nanopore Technologies reveals platform-specific error patterns.. Genome Res. 32(4):726-737.
2018
Tilgner H, Jahanbani F, Gupta I, Collier P, Wei E, Rasmussen M, Snyder M.  2018.  Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome.. Genome Res. 28(2):231-242.
2016
Li S, Garrett-Bakelman FE, Chung SS, Sanders MA, Hricik T, Rapaport F, Patel J, Dillon R, Vijay P, Brown AL et al..  2016.  Distinct evolution and dynamics of epigenetic and genetic heterogeneity in acute myeloid leukemia.. Nat Med. 22(7):792-9.