Michael Schnall-Levin

10X Genomics (United States) — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

17h-index12.8kcitations28works0.02yr avg
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Research Topics

Cancer Genomics and Diagnostics(14), Genomics and Phylogenetic Studies(9), RNA and protein synthesis mechanisms(6), Single-cell and spatial transcriptomics(6), MicroRNA in disease regulation(4)

Publications28 total

Resolving the full spectrum of human genome variation using Linked-Reads
Genome Research·2019· 291 citedOpen Access
Joint single cell DNA-Seq and RNA-Seq of cancer reveals subclonal signatures of genomic instability and gene expression
2018· 19 citedOpen Access
Abstract 281: Identifying genetic variation and cellular heterogeneity with a comprehensive cancer analysis toolkit
Cancer Research·2018
Abstract 3395: A scalable microfluidic platform for determining cellular heterogeneity by copy number detection
Cancer Research·2018
Abstract 3400: Characterizing genomic variation and tumor heterogeneity in cancer
Cancer Research·2018
Resolving the Full Spectrum of Human Genome Variation using Linked-Reads
2017· 40 citedOpen Access
Massively parallel digital transcriptional profiling of single cells
Nature Communications·2017· 7.4k citedOpen Access
Massively parallel digital transcriptional profiling of single cells
2016· 872 citedOpen Access
Abstract 150: Single cell mRNA quantification from 1000s of cells in healthy and malignant tumor samples using a high-throughput droplet-based system
Cancer Research·2016· 2 cited
Abstract 3602: Linked-Reads enable detailed, phased resolution of structural variation in the cancer genome
Cancer Research·2016
Molecular Cytogenetics Using Linked-Reads
Cancer Genetics·2016
Enabling More Complete Genome Analysis Using 10x Linked-Reads
Cancer Genetics·2016
A hybrid approach for de novo human genome sequence assembly and phasing
Nature Methods·2016· 245 citedOpen Access
Health and population effects of rare gene knockouts in adult humans with related parents
Science·2016· 305 citedOpen Access
Haplotyping germline and cancer genomes with high-throughput linked-read sequencing
Nature Biotechnology·2016· 784 citedOpen Access
Health and population effects of rare gene knockouts in adult humans with related parents
2015· 9 citedOpen Access
Extensive sequencing of seven human genomes to characterize benchmark reference materials
2015· 116 citedOpen Access
Abstract 4742: Using 1ng of DNA to detect haplotype phasing and gene fusions from whole exome sequencing of cancer cell lines
Cancer Research·2015
Abstract 4882: Megabase-scale phased haplotypes of genetic aberrations from whole cancer genome sequencing of primary colorectal tumors
Cancer Research·2015
A transgenic resource for conditional competitive inhibition of conserved Drosophila microRNAs
Nature Communications·2015· 87 citedOpen Access
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Frequent Co-authors

Kristina Giorda(10), Rajiv Bharadwaj(9), Sofia Kyriazopoulou-Panagiotopoulou(7), Patrick Marks(7), Heather Ordonez(7), Grace Zheng(6), Kamila Belhocine(6), Claudia Catalanotti(6), Deanna M. Church(6), Jessica M. Terry(5), Zachary Bent(5), Tobias D. Wheeler(5), Christopher M. Hindson(5), Andrew Price(5), Cassandra B. Jabara(5), Željko Džakula(5), Bonnie Berger(5), Phillip Belgrader(4), Ryan J. Wilson(4), Joe Shuga(4)