waszak's profile

Recent Activity

• 17:43: posted Regulation of rtt107 recruitment to stalled DNA replication forks by the cullin rtt101 and the rtt109 acetyltransferase.
• 17:42: posted A high-resolution atlas of nucleosome occupancy in yeast
• 15:22: posted Automated generation of heuristics for biological sequence comparison
• 15:17: posted A high-resolution map of transcription in the yeast genome
• 15:16: posted The Transcriptional Landscape of the Yeast Genome Defined by RNA Sequencing
• 15:15: posted A comparison study: applying segmentation to array CGH data for downstream analyses
• 15:13: posted Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability
• 15:12: posted Copy-number variation and association studies of human disease.
• 15:11: posted Integrated detection and population-genetic analysis of SNPs and copy number variation.
• 15:09: posted Genome sequencing and comparative analysis of Saccharomyces cerevisiae strain YJM789
• 15:07: posted Transcript mapping with high-density oligonucleotide tiling arrays
• 15:06: posted Transcript normalization and segmentation of tiling array data.
• 15:04: posted High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.
• 15:03: posted High-resolution mapping of meiotic crossovers and non-crossovers in yeast
• 15:01: posted A robust statistical method for case-control association testing with copy number variation.
• 14:58: posted Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome
• 14:52: posted Mapping and sequencing of structural variation from eight human genomes
• 14:43: posted Unsupervised segmentation of continuous genomic data
• 14:42: posted QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.
• 14:40: posted Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
• 14:39: posted Mutational and selective effects on copy-number variants in the human genome.
• 14:37: posted A high-resolution survey of deletion polymorphism in the human genome
• 14:36: posted Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.
• 14:34: posted Molecular mechanisms for constitutional chromosomal rearrangements in humans.
• 14:32: posted Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
• 14:31: posted Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.
• 14:29: posted Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
• 14:27: posted Diet and the evolution of human amylase gene copy number variation.
• 14:26: posted Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome
• 14:23: posted The Influence of CCL3L1 Gene-Containing Segmental Duplications on HIV-1/AIDS Susceptibility
• 14:22: posted alpha-Synuclein Locus Triplication Causes Parkinson's Disease
• 13:54: posted Systematic assessment of copy number variant detection via genome-wide SNP genotyping.
• 13:53: posted Global variation in copy number in the human genome
• 13:51: posted Fine-scale structural variation of the human genome
• 13:50: posted Large-Scale Copy Number Polymorphism in the Human Genome
• 13:30: posted Reduction of endogenous angiogenesis inhibitors in Bruch's membrane of the submacular region in eyes with age-related macular degeneration.
• 13:23: posted Expression of endostatin in human choroidal neovascular membranes secondary to age-related macular degeneration.
• 13:21: posted Implications of bevacizumab on VEGF and endostatin in human choroidal neovascularization.

• 22:40: posted Effect of polymorphisms within probe-target sequences on olignonucleotide microarray experiments
• 21:05: posted Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes

• 15:25: posted Modeling of DNA microarray data by using physical properties of hybridization

• 20:06: posted A probabilistic generative model for GO enrichment analysis