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Integration of spatial and single-cell data across modalities with weakly linked features.
- Published in:
- Nature Biotechnology, 2024, v. 42, n. 7, p. 1096, doi. 10.1038/s41587-023-01935-0
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- Article
A comparative study of structural variant calling in WGS from Alzheimer's disease families.
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- Life Science Alliance, 2024, v. 7, n. 5, p. 1, doi. 10.26508/lsa.202302181
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- Article
Integrative single-cell analysis of allele-specific copy number alterations and chromatin accessibility in cancer.
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- Nature Biotechnology, 2021, v. 39, n. 10, p. 1259, doi. 10.1038/s41587-021-00911-w
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- Article
Causal inference for heritable phenotypic risk factors using heterogeneous genetic instruments.
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- PLoS Genetics, 2021, v. 17, n. 6, p. 1, doi. 10.1371/journal.pgen.1009575
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- Article
A Mendelian randomization study of the role of lipoprotein subfractions in coronary artery disease.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.58361
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- Article
Surface protein imputation from single cell transcriptomes by deep neural networks.
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- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-14391-0
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- Article
DENDRO: genetic heterogeneity profiling and subclone detection by single-cell RNA sequencing.
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- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-019-1922-x
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- Article
Elite control of HIV is associated with distinct functional and transcriptional signatures in lymphoid tissue CD8<sup>+</sup> T cells.
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- Science Translational Medicine, 2019, v. 11, n. 523, p. 1, doi. 10.1126/scitranslmed.aax4077
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- Article
Bulk tissue cell type deconvolution with multi-subject single-cell expression reference.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08023-x
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- Article
Sensitivity analysis and power for instrumental variable studies.
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- Biometrics, 2018, v. 74, n. 4, p. 1150, doi. 10.1111/biom.12873
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- Article
CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing.
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- Genome Biology, 2018, v. 19, n. 1, p. N.PAG, doi. 10.1186/s13059-018-1578-y
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- Article
DNA copy number profiling using single-cell sequencing.
- Published in:
- Briefings in Bioinformatics, 2018, v. 19, n. 5, p. 731, doi. 10.1093/bib/bbx004
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- Article
SVEngine: an efficient and versatile simulator of genome structural variations with features of cancer clonal evolution.
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- GigaScience, 2018, v. 7, n. 7, p. N.PAG, doi. 10.1093/gigascience/giy081
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- Article
Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny.
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- Bioinformatics, 2018, v. 34, n. 12, p. 2126, doi. 10.1093/bioinformatics/bty057
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- Article
Identification of large rearrangements in cancer genomes with barcode linked reads.
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- Nucleic Acids Research, 2018, v. 46, n. 4, p. e19, doi. 10.1093/nar/gkx1193
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- Article
Learning-dependent chromatin remodeling highlights noncoding regulatory regions linked to autism.
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- Science Signaling, 2018, v. 11, n. 513, p. 1, doi. 10.1126/scisignal.aan6500
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- Article
Functional germline variants as potential co-oncogenes.
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- NPJ Breast Cancer, 2017, v. 3, n. 1, p. N.PAG, doi. 10.1038/s41523-017-0051-5
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- Article
Accounting for technical noise in differential expression analysis of single-cell RNA sequencing data.
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- Nucleic Acids Research, 2017, v. 45, n. 19, p. 10978, doi. 10.1093/nar/gkx754
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- Article
BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00388-9
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- Article
Corrigendum: Allelic variation contributes to bacterial host specificity.
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- Nature Communications, 2017, v. 8, n. 8, p. 15229, doi. 10.1038/ncomms15229
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- Article
SCALE: modeling allele-specific gene expression by single-cell RNA sequencing.
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- Genome Biology, 2017, v. 18, p. 1, doi. 10.1186/s13059-017-1200-8
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- Article
A genome-wide approach for detecting novel insertion-deletion variants of mid-range size.
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- Nucleic Acids Research, 2016, v. 44, n. 15, p. 1, doi. 10.1093/nar/gkw481
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- Article
Global copy number profiling of cancer genomes.
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- Bioinformatics, 2016, v. 32, n. 6, p. 926, doi. 10.1093/bioinformatics/btv676
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- Article
Emergence of Hemagglutinin Mutations During the Course of Influenza Infection.
- Published in:
- Scientific Reports, 2015, p. 16178, doi. 10.1038/srep16178
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- Article
Allelic variation contributes to bacterial host specificity.
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- Nature Communications, 2015, v. 6, n. 10, p. 8754, doi. 10.1038/ncomms9754
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- Article
Memory acquisition and retrieval impact different epigenetic processes that regulate gene expression.
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- BMC Genomics, 2015, v. 16, p. 1, doi. 10.1186/1471-2164-16-S5-S5
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- Article
CODEX: a normalization and copy number variation detection method for whole exome sequencing.
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- Nucleic Acids Research, 2015, v. 43, n. 6, p. 1, doi. 10.1093/nar/gku1363
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- Article
Allele-specific copy number profiling by next-generation DNA sequencing.
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- Nucleic Acids Research, 2015, v. 43, n. 4, p. 1, doi. 10.1093/nar/gku1252
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- Article
Metastatic tumor evolution and organoid modeling implicate TGFBR2 as a cancer driver in diffuse gastric cancer.
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- Genome Biology, 2014, v. 15, n. 7, p. 28, doi. 10.1186/s13059-014-0428-9
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- Article
False discovery rates and copy number variation.
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- Biometrika, 2011, v. 98, n. 2, p. 251, doi. 10.1093/biomet/asr018
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- Article
Estimation of Parent Specific DNA Copy Number in Tumors using High-Density Genotyping Arrays.
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- PLoS Computational Biology, 2011, v. 7, n. 1, p. 1, doi. 10.1371/journal.pcbi.1001060
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- Article
Detecting simultaneous changepoints in multiple sequences.
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- Biometrika, 2010, v. 97, n. 3, p. 631, doi. 10.1093/biomet/asq025
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Joint estimation of DNA copy number from multiple platforms.
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- Bioinformatics, 2010, v. 26, n. 2, p. 153, doi. 10.1093/bioinformatics/btp653
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- Article
A Modified Bayes Information Criterion with Applications to the Analysis of Comparative Genomic Hybridization Data.
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- Biometrics, 2007, v. 63, n. 1, p. 22, doi. 10.1111/j.1541-0420.2006.00662.x
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- Article