Found: 19
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Multi-omics signatures of the human early life exposome.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34422-2
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- Publication type:
- Article
MultiDataSet: an R package for encapsulating multiple data sets with application to omic data integration.
- Published in:
- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-016-1455-1
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- Publication type:
- Article
In utero and childhood exposure to tobacco smoke and multi-layer molecular signatures in children.
- Published in:
- 2020
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- Publication type:
- journal article
Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.65310
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- Publication type:
- Article
Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.65310
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- Publication type:
- Article
affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling.
- Published in:
- BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0608-y
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- Publication type:
- Article
A systemic approach to identify signaling pathways activated during short-term exposure to traffic-related urban air pollution from human blood.
- Published in:
- Environmental Science & Pollution Research, 2018, v. 25, n. 29, p. 29572, doi. 10.1007/s11356-018-3009-8
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- Publication type:
- Article
Correction to: A guide to writing systematic reviews of rare disease treatments to generate FAIRcompliant datasets: building a Treatabolome.
- Published in:
- 2021
- By:
- Publication type:
- corrected article
A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Variability of multi-omics profiles in a population-based child cohort.
- Published in:
- 2021
- By:
- Publication type:
- journal article
The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases.
- Published in:
- Human Mutation, 2022, v. 43, n. 6, p. 717, doi. 10.1002/humu.24353
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- Publication type:
- Article
The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.
- Published in:
- Human Mutation, 2020, v. 41, n. 2, p. 387, doi. 10.1002/humu.23942
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- Publication type:
- Article
Comparative analysis of whole-genome sequencing pipelines to minimize false negative findings.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39108-2
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- Publication type:
- Article
Association between the pregnancy exposome and fetal growth.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Comprehensive study of the exposome and omic data using rexposome Bioconductor Packages.
- Published in:
- Bioinformatics, 2019, v. 35, n. 24, p. 5344, doi. 10.1093/bioinformatics/btz526
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- Publication type:
- Article
CTDquerier: a bioconductor R package for Comparative Toxicogenomics DatabaseTM data extraction, visualization and enrichment of environmental and toxicological studies.
- Published in:
- Bioinformatics, 2018, v. 34, n. 18, p. 3235, doi. 10.1093/bioinformatics/bty326
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- Publication type:
- Article
psygenet2r: a R/Bioconductor package for the analysis of psychiatric disease genes.
- Published in:
- Bioinformatics, 2017, v. 33, n. 24, p. 4004, doi. 10.1093/bioinformatics/btx506
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- Publication type:
- Article
Circulating miRNAs, isomiRs and small RNA clusters in human plasma and breast milk.
- Published in:
- PLoS ONE, 2018, v. 13, n. 3, p. 1, doi. 10.1371/journal.pone.0193527
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- Publication type:
- Article
WEScover: selection between clinical whole exome sequencing and gene panel testing.
- Published in:
- BMC Bioinformatics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12859-021-04178-5
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- Publication type:
- Article