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The HapMap project

Table of Contents: “…Contents: The problem in pedigree analysis -- A possible solution for the resolution limitations in pedigree analysis -- Theory of two loci -- Linkage equilibrium and disequilibrium -- Recombination events between SNPs -- Genealogical interpretation -- Statistical significance of LD -- The effect of random drift on linkage disequilibrium -- Variability of LD among different populations -- Heterogeneity of LD across the genome -- Hotspots of recombination -- Tag SNPs -- The HapMap website -- Design of GWAS -- Welcome Trust Case Control Consortium -- Etiology.…”
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The future of CNVs sequence based resolution and links to human disease, part 1 of 2 /

Table of Contents: “…Contents: Human genetic variation -- "Normal" structural variation -- Copy number polymorphism and disease -- Duplicated sequences: copy number variant (CNV) hotspots -- Structural variation and enriched gene functions -- Array comparative genomic hybridization -- Insufficiency of CNV detection -- Sequence-based resolution of structural variation -- Genome-wide detection of structural variation -- Validated sites of structural variation -- Frequency and length distribution -- APOBEC3B -- Breakpoint heterogeneity -- Detection of novel insertion sequences.…”
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Series (Copy number variation)
Series (Biomarkers)