06 | Drug score distributions for the ten most-prescribed drugs in the 1000 Depressives. | TopicSem |
12 | SATIE: a web tool to predict sequential treatments in cancer. | xMutant | ||
28 | Profiling and leveraging relatedness in a precision medicine cohort of 92,455 exomes | J.Club |
25 | Variants associated with an increased risk for severe neutropenia in patients receiving 6MP. | TopicSem |
17 | Identification of variants with a significantly lower frequency in cases than in controls | TopicSem |
15 | VVA: Gene-centered Visualization and Annotation for Exome Variant Analysis | TopicSem |
13 | Association of ADRA1A polymorphism with Ritodrine-induced Pulmonary Edema in 13 pregnant women. | TopicSem | ||
22 | Preprocessing and QC results of 119 ALL WXSs. | xMutant |
02 | Variant Visualization and Annotation Tool Available Online | TopicSem | ||
02 | Public genome databases: GnomDB, ExAC and ESP6500. | xMutant |
22 | Genetic Variation Among 82 Pharmacogenes: The PGRNseq Data From the eMERGE Network | J.Club |
05 | CRAM format - An efficiently compressed BAM file | xMutant | ||
07 | Depression WXS QC - 10 samples of FASTQ from Illumina HiSeq 2500 | TopicSem |
19 | Whole-exome sequencing to detect significantly altered genes causing Ritodrine induced side effects in 13 pregnant women. | Seminar |
20 | Comparison between the results of NGS and SNP Type Assays | TopicSem |
04 | Evaluation of filtering strategies to identify disease-associated genomic variants in multiple disease categories. | TopicSem |
19 | BOOGIE: Predicting Blood Groups from High Throughput Sequencing Data | J.Club | ||
23 | Ritodrine meta-pathway and sub-pathway scores. | TopicSem |
11 | Matched-pair analysis of a breast cancer patient. | TopicSem | ||
13 | Preprocessing and QC results of 27 BronJ WXSs. | xMutant |
12 | [Journal review] Informatics for RNA Sequencing | xMutant |
19 | Targeted sequencing to detect abnormalities causing Yutopar side effects in 11 pregnant women | TopicSem |
04 | Investigation of systematic errors of called variants through alignment viewer. | TopicSem | ||
05 | Taking a snapshot of aligned reads and IGV batch job scripts | xMutant |
01 | Characteristics of genes with rare and deleterious mutations in 1KP samples | TopicSem | ||
13 | HTSeq-a Python framework to work with high-throughput sequencing data | J.Club |
28 | Distribution characteristics of genes with rare and deleterious mutations in 1KP | xMutant |
12 | WXS analysis of 6-mercaptopurine related neutropenia cases from ALL | xMutant | ||
22 | WXS analysis of 6-mercaptopurine related neutropenia cases from ALL | TopicSem |
10 | Association Study: Cancer Risk Alleles from GWAS and Rare Mutations | TopicSem |
23 | Damaged Gene and Exon Scores for 1000 Genomes Project | TopicSem | ||
28 | Signatures of mutational processes in human cancer | J.Club |
21 | The Distribution of Somatic Mutations in POLE and POLD1. | TopicSem | ||
24 | The Exomes of the NCI-60 Panel: A Genomic Resource for Cancer Biology and Systems Pharmacology | J.Club |
04 | Signature of Nephrotic Syndrome | Seminar |
07 | Blood genotyping for pretransfusion testing | SysBiol | ||
10 | In silico blood genotyping from exome sequencing data | J.Club | ||
14 | Blood genotyping for pretransfusion testing. | TopicSem |
31 | RNA-seq analysis: Label miss matched, Differentially Expressed Isoforms. | TopicSem |
26 | RNA-Seq Analysis: how to handle missing values? | TopicSem |
25 | Reads align with Bowtie2 | SysBiol | ||
30 | RNA-seq reads alignment with Bowtie2. | TopicSem |
27 | Comparison of RNA data analysis results: Cuffdiff algorithm validation. | TopicSem | ||
30 | A high-resolution map of human evolutionary constraint using 29 mammals | J.Club |
18 | Loss of Function Gene-set Analysis Of Personal Genome Using Pathway-Disease Similarity. | TopicSem | ||
28 | Detecting and annotating genetic variations using the HugeSeq pipeline. | J.Club |
01 | Phenotypic signature practicality. | SysBiol | ||
07 | Stablishing phenotypic signatures to infer relevant phenotypic characteristics using semantic similarity calculation | Seminar |
04 | Construct a Network Linking Personal Variations | xMutant | ||
31 | Genome Browser - Browsing SNUBI Sequences. | TopicSem |
11 | Gene-set wise approach for disease susceptibility using SNP profiles. | TopicSem | ||
21 | Rare Disease Knowledgebase and Exome Sequence Data | SysBiol |
14 | Discovery of common Asian copy number variants using integrated high-resolution arrayCGH and massively parallel DNA sequencing | BioEMR |
23 | Targeted capture and massively parallel sequencing of 12 human exomes | MAInfo |
15 | Signup_Procedure | BioEMR | ||
19 | Generations of sequencing technologies | MAInfo | ||
28 | CCR Plus App Bugs Report | BioEMR |
13 | CCR Plus Database Schema | BioEMR | ||
13 | Rare Disease Input Data Analysis | BioEMR | ||
20 | RE:CCR Plus Database Schema | BioEMR | ||
20 | Rare_Disease_ Step1. | BioEMR | ||
23 | Rare_Disease_Knowledge_Base | Seminar |
23 | Relations in biomedical ontologies | BioEMR | ||
30 | Relations in biomedical ontolodies | BioEMR |