20:17
Paul Medvedev - The minimizer Jaccard estimator is biased and inconsistent
29:37
Tizian Schulz - Sequence-based Pangenomic Core Detection
11:18
Kristoffer Sahlin - Flexible seed size enables ultra-fast and accurate read alignment
19:35
Giulio Ermanno Pibiri - Sparse and Skew Hashing of K-Mers
15:09
Ivan Tolstoganov - BinSPreader: refine binning results for fuller MAG reconstruction
18:52
Yuwei Bao-Real Time Direct Classification of Nanopore signals with SquiggleNet
20:20
Timothy Barry-Conditional resampling improves calibration and sensitivity in single cell CRISPR scre
18:54
Luca Renders-Dynamic Partitioning of Search Patterns for Approximate Pattern Matching using Search S
01:12:54
Keynote-Nadia Pisanti-ReadMapping on Pan Genomes with Degenerate Texts
19:46
Tuukka Norri-Algorithms and Complexity on Indexing Founder Graphs
20:47
Norbert Dojer-Linearization of genome sequence graphs revisited
19:44
Omar Ahmed-Pan genomic matching statistics for targeted nanopore sequencing
22:37
Ali Heydari-ACTIVA realistic single cell RNA seq generation with automatic cell type identification
20:45
Jixing Chen-DeepDRIM a deep neural network to reconstruct cell type specific gene regulatory network
19:02
Eleonora Rachtman-Accurate contamination removal using locality sensitive hashing
21:19
Riccardo Vicedomini-Automated strain separation in low complexity metagenomics using long reads
20:30
Peter Nguyen-A molecular taxonomy of tumors independent of tissue of origin
22:04
Matthew Hayes -HolistIC leveraging Hi-C and whole genome shotgun sequencing for double minute chrms
20:41
Ziwei Chen-BiTSC2 Bayesian Inference of Tumor clonal Tree by joint analysis of single cell SNV & ...
01:00:51
Keynote-Ben Langmead-Pan genomic methods for fighting reference bias
22:13
Lauren Mak-Ariadne: Barcoded Linked-Read Deconvolution Using de Bruijn Graphs
19:06
Raja Appuswamy-Accel-Align a fast sequence mapper and aligner based on the seed-embed-extend method
21:26
Kristoffer Sahlin - Accurate spliced alignment of long RNA sequencing reads
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About
RECOMB-seq was founded in 2011 as a response to the expanding applications of high-throughput sequencing as a tool of basic science and biomedicine. The conference gathered leading researchers in computational genomics and genomic biology to discuss emerging frontiers in algorithm development for sequencing data. The emphasis is on applying computational approaches to improve analysis, interpretation and data management. Since then, the scope of RECOMB-seq has expanded beyond sequencing data to include assembled data as well, all the while focusing on methodological developments.
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