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Assembly and analysis of the genome of Notholithocarpus densiflorus.
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- G3: Genes | Genomes | Genetics, 2024, v. 14, n. 5, p. 1, doi. 10.1093/g3journal/jkae043
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- Article
Accurate haplotype-resolved assembly reveals the origin of structural variants for human trios.
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- Bioinformatics, 2021, v. 37, n. 15, p. 2095, doi. 10.1093/bioinformatics/btab068
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- Article
Comparison of long-read methods for sequencing and assembly of a plant genome.
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- GigaScience, 2020, v. 9, n. 12, p. 1, doi. 10.1093/gigascience/giaa146
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- Article
TGS-GapCloser: A fast and accurate gap closer for large genomes with low coverage of error-prone long reads.
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- GigaScience, 2020, v. 9, n. 9, p. 1, doi. 10.1093/gigascience/giaa094
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- Article
IterCluster: a barcode clustering algorithm for long fragment read analysis.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.8431
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- Article
On the ubiquity of electromagnetic-duality rotations in 4D, 𝒩=1 holoraumy tensors for on-shell 4D supermultiplets.
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- International Journal of Modern Physics A: Particles & Fields; Gravitation; Cosmology; Nuclear Physics, 2020, v. 35, n. 1, p. N.PAG, doi. 10.1142/S0217751X20500086
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- Article
An ATAC-seq atlas of chromatin accessibility in mouse tissues.
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- Scientific Data, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41597-019-0071-0
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- Article
Significant abundance of cis configurations of coding variants in diploid human genomes.
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- Nucleic Acids Research, 2019, v. 47, n. 6, p. 2981, doi. 10.1093/nar/gkz031
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- Article
3′ Branch ligation: a novel method to ligate non-complementary DNA to recessed or internal 3′OH ends in DNA or RNA.
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- DNA Research, 2019, v. 26, n. 1, p. 45, doi. 10.1093/dnares/dsy037
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- Article
Advanced Whole-Genome Sequencing and Analysis of Fetal Genomes from Amniotic Fluid.
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- Clinical Chemistry, 2018, v. 64, n. 4, p. 715, doi. 10.1373/clinchem.2017.281220
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- Article
Novel genetic risk variants for pediatric celiac disease.
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- Human Genomics, 2016, v. 10, p. 1, doi. 10.1186/s40246-016-0091-1
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- Article
The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes.
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- GigaScience, 2016, v. 5, p. 1, doi. 10.1186/s13742-016-0148-z
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- Article
Whole genome sequence analysis of BT- 474 using complete Genomics' standard and long fragment read technologies.
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- GigaScience, 2016, v. 5, p. 1, doi. 10.1186/s13742-016-0113-x
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- Article
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
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- Human Genomics, 2015, v. 9, n. 1, p. 1, doi. 10.1186/s40246-015-0034-2
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- Article
Accurate Whole Genome Sequencing as the Ultimate Genetic Test.
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- Clinical Chemistry, 2015, v. 61, n. 1, p. 305, doi. 10.1373/clinchem.2014.224907
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- Article
Co-barcoded sequence reads from long DNA fragments: a cost-effective solution for "perfect genome" sequencing.
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- Frontiers in Genetics, 2015, v. 5, p. 1, doi. 10.3389/fgene.2014.00466
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- Article
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autism.
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- Nature Genetics, 2013, v. 45, n. 11, p. 1405, doi. 10.1038/ng.2776
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Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells.
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- Nature, 2012, v. 487, n. 7406, p. 190, doi. 10.1038/nature11236
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- Article
Deep RNA sequencing analysis of readthrough gene fusions in human prostate adenocarcinoma and reference samples.
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- BMC Medical Genomics, 2011, v. 4, n. 1, p. 11, doi. 10.1186/1755-8794-4-11
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- Article
Diverse somatic mutation patterns and pathway alterations in human cancers.
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- Nature, 2010, v. 466, n. 7308, p. 869, doi. 10.1038/nature09208
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- Article
Highly efficient somatic-mutation identification using Escherichia coli mismatch-repair detection.
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- Nature Methods, 2007, v. 4, n. 9, p. 713, doi. 10.1038/nmeth1081
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Pharmacologic and Toxicologic Evaluation of C. novyi-NT Spores.
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- Toxicological Sciences, 2005, v. 88, n. 2, p. 562, doi. 10.1093/toxsci/kfi316
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- Article
Contribution of bone marrow-derived endothelial cells to human tumor vasculature.
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- Nature Medicine, 2005, v. 11, n. 3, p. 261, doi. 10.1038/nm1200
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- Article
Transcriptome PETs: A genome's best friends.
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- Nature Methods, 2005, v. 2, n. 2, p. 93, doi. 10.1038/nmeth0205-93
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- Article