Source: Bioethics in Asia : Proceedings of the UNESCO Asian Bioethics Conference (ABC'97) and the WHo-assisted Satellite Symposium on Medical Genettes Services / Fujiki, N. & Macer, D.R.J. (ed.), (1998) p.

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Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Authors : Birney, Ewan; The ENCODE Project Consortium;

Subjects: info:eu-repo/classification/ddc/576.5; Chromatin/genetics/metabolism; Chromatin Immunoprecipitation

Source: ISSN: 0028-0836 ; Nature, vol. 447, no. 7146 (2007) p. 799-816.

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A map of human genome variation from population-scale sequencing

Authors : 1000 Genomes Project Consortium; Dermitzakis, Emmanouil

Subjects: info:eu-repo/classification/ddc/576.5; Calibration; Chromosomes

Source: ISSN: 0028-0836 ; Nature, vol. 467, no. 7319 (2010) p. 1061-1073.

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Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies

Authors : Panousis, Nikolaos; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil

Subjects: info:eu-repo/classification/ddc/576.5; Chromosome Mapping; Genetic Association Studies

Source: ISSN: 1465-6906 ; GenomeBiology.com, vol. 15, no. 9 (2014) 467.

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Genome-sequencing anniversary. Genome literacy

Authors : Dermitzakis, Emmanouil

Subjects: info:eu-repo/classification/ddc/576.5; Gene Expression Regulation; Genetic Variation

Source: ISSN: 0036-8075 ; Science, vol. 331, no. 6018 (2011) p. 689-690.

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Integrating common and rare genetic variation in diverse human populations

Authors : Altshuler, D. M.;

Subjects: info:eu-repo/classification/ddc/576.5; DNA Copy Number Variations; Genome

Source: ISSN: 0028-0836 ; Nature, vol. 467, no. 7311 (2010) p. 52-58.

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A gene desert required for regulatory control of pleiotropic Shox2 expression and embryonic survival

Authors : Abassah-Oppong, Samuel; Zoia, Matteo; Mannion, Brandon J

Subjects: info:eu-repo/classification/ddc/590; info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/576.5

Source: ISSN: 2041-1723 ; Nature communications, vol. 15, no. 1 (2024) 8793.

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فلترة النتائج

High-resolution mapping of mitotic DNA synthesis regions and common fragile sites in the human genome through direct sequencing

Replication of the principal component analyses of the human genome diversity panel

DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome

The human genome : metaphysical object and political icon

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

A map of human genome variation from population-scale sequencing

Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies

Genome-sequencing anniversary. Genome literacy

Integrating common and rare genetic variation in diverse human populations

A gene desert required for regulatory control of pleiotropic Shox2 expression and embryonic survival

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