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Evidence for the Association between the Intronic Haplotypes of Ionotropic Glutamate Receptors and First-Episode Schizophrenia.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 12, p. 1250, doi. 10.3390/jpm11121250
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- Publication type:
- Article
Chromatin accessibility landscape of pediatric T‐lymphoblastic leukemia and human T‐cell precursors.
- Published in:
- EMBO Molecular Medicine, 2020, v. 12, n. 9, p. 1, doi. 10.15252/emmm.202012104
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- Publication type:
- Article
PDX models recapitulate the genetic and epigenetic landscape of pediatric T‐cell leukemia.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 12, p. N.PAG, doi. 10.15252/emmm.201809443
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- Publication type:
- Article
Genomic structural variations lead to dysregulation of important coding and non‐coding RNA species in dilated cardiomyopathy.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 1, p. 107, doi. 10.15252/emmm.201707838
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- Publication type:
- Article
Tracy: basecalling, alignment, assembly and deconvolution of sanger chromatogram trace files.
- Published in:
- BMC Genomics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12864-020-6635-8
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- Publication type:
- Article
The effects of common structural variants on 3D chromatin structure.
- Published in:
- BMC Genomics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12864-020-6516-1
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- Publication type:
- Article
Coordinated expression and genetic polymorphisms in Grainyhead-like genes in human non-melanoma skin cancers.
- Published in:
- 2018
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- Publication type:
- journal article
Functional analysis of structural variants in single cells using Strand-seq.
- Published in:
- Nature Biotechnology, 2023, v. 41, n. 6, p. 832, doi. 10.1038/s41587-022-01551-4
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- Publication type:
- Article
Single-cell analysis of structural variations and complex rearrangements with tri-channel processing.
- Published in:
- Nature Biotechnology, 2020, v. 38, n. 3, p. 343, doi. 10.1038/s41587-019-0366-x
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- Publication type:
- Article
A highly soluble Sleeping Beauty transposase improves control of gene insertion.
- Published in:
- Nature Biotechnology, 2019, v. 37, n. 12, p. 1502, doi. 10.1038/s41587-019-0291-z
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- Publication type:
- Article
Assembly and diploid architecture of an individual human genome via single-molecule technologies.
- Published in:
- Nature Methods, 2015, v. 12, n. 8, p. 780, doi. 10.1038/nmeth.3454
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- Publication type:
- Article
TRiCoLOR: tandem repeat profiling using whole-genome long-read sequencing data.
- Published in:
- GigaScience, 2020, v. 9, n. 10, p. 1, doi. 10.1093/gigascience/giaa101
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- Publication type:
- Article
Mitoferrin2 is a synthetic lethal target for chromosome 8p deleted cancers.
- Published in:
- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01357-w
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- Publication type:
- Article
Multi-platform discovery of haplotype-resolved structural variation in human genomes.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-018-08148-z
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- Publication type:
- Article
Metagenomic analysis of primary colorectal carcinomas and their metastases identifies potential microbial risk factors.
- Published in:
- Molecular Oncology, 2021, v. 15, n. 12, p. 3363, doi. 10.1002/1878-0261.13070
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- Publication type:
- Article
Robust consensus computation.
- Published in:
- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-S10-P4
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- Publication type:
- Article
SeqAn An efficient, generic C++ library for sequence analysis.
- Published in:
- 2008
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- Publication type:
- Product Review
The Relation between Parents' Child-Rearing Behavior and Their Socioeconomic Status in a Developing Country Context: A Case from West Bengal, India.
- Published in:
- Zeitschrift für Internationale Bildungsforschung und Entwicklungspädagogik, 2020, v. 43, n. 2, p. 33, doi. 10.31244/zep.2020.02.06
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- Publication type:
- Article
MEDU-11. MOLECULAR CHARACTERIZATION OF ETMRs REVEALS A ROLE FOR R-LOOP MEDIATED CHROMOSOMAL INSTABILITY.
- Published in:
- Neuro-Oncology, 2019, v. 21, p. ii105, doi. 10.1093/neuonc/noz036.170
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- Publication type:
- Article
Identification of novel sequence variations in microRNAs in chronic lymphocytic leukemia.
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- Carcinogenesis, 2014, v. 35, n. 5, p. 992, doi. 10.1093/carcin/bgt396
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- Publication type:
- Article
Characterization of Two Historic Smallpox Specimens from a Czech Museum.
- Published in:
- Viruses (1999-4915), 2017, v. 9, n. 8, p. 200, doi. 10.3390/v9080200
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- Publication type:
- Article
Genomic insights into the pathogenesis of Epstein–Barr virus-associated diffuse large B-cell lymphoma by whole-genome and targeted amplicon sequencing.
- Published in:
- Blood Cancer Journal, 2021, v. 11, n. 5, p. 1, doi. 10.1038/s41408-021-00493-5
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- Publication type:
- Article
Potential protective role of Grainyhead-like genes in the development of clear cell renal cell carcinoma.
- Published in:
- Molecular Carcinogenesis, 2017, v. 56, n. 11, p. 2414, doi. 10.1002/mc.22682
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- Publication type:
- Article
An integrated map of structural variation in 2,504 human genomes.
- Published in:
- Nature, 2015, v. 526, n. 7571, p. 75, doi. 10.1038/nature15394
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- Publication type:
- Article
Dissecting the genomic complexity underlying medulloblastoma.
- Published in:
- Nature, 2012, v. 488, n. 7409, p. 100, doi. 10.1038/nature11284
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- Publication type:
- Article
Corrigendum: Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma.
- Published in:
- 2012
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- Publication type:
- Erratum
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma.
- Published in:
- Nature, 2012, v. 482, n. 7384, p. 226, doi. 10.1038/nature10833
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- Publication type:
- Article
Identification of cytokine-induced modulation of microRNA expression and secretion as measured by a novel microRNA specific qPCR assay.
- Published in:
- Scientific Reports, 2015, p. 11590, doi. 10.1038/srep11590
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- Publication type:
- Article
ICGC PedBrain - dissecting the genomic complexity underlying medulloblastoma using whole-genome sequencing.
- Published in:
- 2012
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- Publication type:
- Abstract
ToTem: a tool for variant calling pipeline optimization.
- Published in:
- BMC Bioinformatics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12859-018-2227-x
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- Publication type:
- Article
MCM3AP and POMP Mutations Cause a DNA-Repair and DNA-Damage-Signaling Defect in an Immunodeficient Child.
- Published in:
- Human Mutation, 2016, v. 37, n. 3, p. 257, doi. 10.1002/humu.22939
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- Publication type:
- Article
Impact and characterization of serial structural variations across humans and great apes.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52027-9
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- Publication type:
- Article
VISOR: a versatile haplotype-aware structural variant simulator for short- and long-read sequencing.
- Published in:
- Bioinformatics, 2020, v. 36, n. 4, p. 1267, doi. 10.1093/bioinformatics/btz719
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- Publication type:
- Article
Alfred: interactive multi-sample BAM alignment statistics, feature counting and feature annotation for long- and short-read sequencing.
- Published in:
- Bioinformatics, 2019, v. 35, n. 14, p. 2489, doi. 10.1093/bioinformatics/bty1007
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- Publication type:
- Article
DELLY: structural variant discovery by integrated paired-end and split-read analysis.
- Published in:
- Bioinformatics, 2012, v. 28, n. 18, p. i333, doi. 10.1093/bioinformatics/bts378
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- Publication type:
- Article
A consistency-based consensus algorithm for de novo and reference-guided sequence assembly of short reads.
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- Bioinformatics, 2009, v. 25, n. 9, p. 1118, doi. 10.1093/bioinformatics/btp131
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- Publication type:
- Article
Segment-based multiple sequence alignment.
- Published in:
- Bioinformatics, 2008, v. 24, n. 16, p. i187, doi. 10.1093/bioinformatics/btn281
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- Publication type:
- Article