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Author Details
Full Name
David Tse
Affiliation
Stanford University
ORCID
Career Start Year
2013
Papers
19
H Index
11
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37961606
OASIS: An interpretable, finite-sample valid alternative to Pearson's <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:msup><mml:mrow><mml:mi>X</mml:mi></mml:mrow><mml:mrow><mml:mn>2</mml:mn></mml:mrow></mml:msup></mml:math> for scientific discovery.
bioRxiv
2023
32484809
RefShannon: A genome-guided transcriptome assembler using sparse flow decomposition.
PLoS One
2020
32034137
Determining sequencing depth in a single-cell RNA-seq experiment.
Nat Commun
2020
33205128
Spectral Jaccard Similarity: A New Approach to Estimating Pairwise Sequence Alignments.
Patterns (N Y)
2020
31142858
Longitudinal multi-omics of host-microbe dynamics in prediabetes.
Nature
2019
31359007
Large dataset enables prediction of repair after CRISPR-Cas9 editing in primary T cells.
Nat Biotechnol
2019
31521605
Valid Post-clustering Differential Analysis for Single-Cell RNA-Seq.
Cell Syst
2019
31042711
Somatic mutations render human exome and pathogen DNA more similar.
PLoS One
2019
29523077
An interpretable framework for clustering single-cell RNA-Seq datasets.
BMC Bioinformatics
2018
29422526
Optimal compressed representation of high throughput sequence data via light assembly.
Nat Commun
2018
29700301
Publisher Correction: Optimal compressed representation of high throughput sequence data via light assembly.
Nat Commun
2018
28025204
Novel probabilistic models of spatial genetic ancestry with applications to stratification correction in genome-wide association studies.
Bioinformatics
2017
28320918
HINGE: long-read assembly achieves optimal repeat resolution.
Genome Res
2017
27230763
Fast and accurate single-cell RNA-seq analysis by clustering of transcript-compatibility counts.
Genome Biol
2016
27587667
Information-optimal genome assembly via sparse read-overlap graphs.
Bioinformatics
2016
26040454
FinisherSC: a repeat-aware tool for upgrading de novo assembly using long reads.
Bioinformatics
2015
27135798
Fundamental Limits of Search.
Cell Syst
2015
25252708
Near-optimal assembly for shotgun sequencing with noisy reads.
BMC Bioinformatics
2014
23902516
Optimal assembly for high throughput shotgun sequencing.
BMC Bioinformatics
2013
1 - 19 of 19
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