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Making the difference: integrating structural variation detection tools.

• Authors : Ke Lin¹; Smit, Sandra²; Bonnema, Guusje³

Subjects: HUMAN genetic variation; EUKARYOTES; PHENOTYPES

• Source: Briefings in Bioinformatics. Sep2015, Vol. 16 Issue 5, p852-864. 13p.

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Your genetic destiny for sale.

• Authors : Taubes, Gary

Subjects: POPULATION genetics; CHRONIC diseases; DNANEWFOUND Genomics (Company)

• Source: Technology Review. Apr2001, Vol. 104 Issue 3, p40. 7p. 1 Chart.

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Public data and open source tools for multi-assay genomic investigation of disease.

• Authors : Kannan, Lavanya¹; Ramos, Marcel²; Re, Angela³

Subjects: *OPEN source software; GENOMICS; NUCLEOTIDE sequencingBIOCONDUCTOR (Computer software)

• Source: Briefings in Bioinformatics. Jul2016, Vol. 17 Issue 4, p603-615. 13p.

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Alignment-free phylogenetics and population genetics.

• Authors : Haubold, Bernhard

Subjects: PHYLOGENY; POPULATION genetics; GENETIC mutation

• Source: Briefings in Bioinformatics. May2014, Vol. 15 Issue 3, p407-418. 12p.

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new approach to decode DNA methylome and genomic variants simultaneously from double strand bisulfite sequencing.

• Authors : Liang, Jialong¹ (AUTHOR); Zhang, Kun² (AUTHOR); Yang, Jie² (AUTHOR)

Subjects: DNA; DNA methylation; PROMOTERS (Genetics)

• Source: Briefings in Bioinformatics. Nov2021, Vol. 22 Issue 6, p1-10. 10p.

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Be Wary of Mixing Race and Medicine.

Subjects: ETHNOLOGY; DRUG development; GENOMICSUNITED States

• Source: Technology Review. Apr2005, Vol. 108 Issue 4, p18-18. 1p. 1 Color Photograph.

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Partnering.

• Authors : HARN, JAY

• Source: San Diego Business Journal. 7/27/2020, Vol. 41 Issue 30, p3-3. 1/4p.

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