AGAAT: Automated computational tool integrating different genotyping array and correctional methods for data analysis
Prakash, A.; Banerjee, M.
Show abstract
Genotyping arrays are widely used in studying the genetics of complex diseases. Arrays with multi-ethnic markers enable population-scale and cost-effective genetic studies in underrepresented populations. But automated pipelines that convert raw data files into association results are lacking for these genotyping arrays. Also, combining variant files from multiple genotyping projects is difficult due to differences arising from multiple versions of standard file formats like Variant Calling Format (VCF). We have developed an automated tool named AGAAT (Automated Genotyping Array Analysis Tool) to overcome these problems. In addition to the automated pipelines for multi-ethnic arrays, we have added additional Python scripts for multiple testing correction using haplotype blocks, candidategene analysis, candidate-gene common-variant analysis and addition of 1000 genome phase-3 genotype counts to the controls, followed by case-control association analysis.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Comparative analysis of novel MGISEQ-2000 sequencing platform vs Illumina HiSeq 2500 for whole-genome sequencing 95%
- ChatGPT-Enhanced ROC Analysis (CERA): A Shiny Web Tool for Finding Optimal Cutoff in Biomarker Analysis 95%
- NGSpop: A desktop software that supports population studies by identifying sequence variations from next-generation sequencing data 95%
Similar papers in this journal
- Variant Graph Craft (VGC): A Comprehensive Tool for Analyzing Genetic Variation and Identifying Disease-Causing Variants. 94%
- Rare Copy Number Variant analysis in case-control studies using SNP Array Data: a scalable and automated data analysis pipeline 94%
- H3AGWAS : A portable workflow for Genome Wide Association Studies 94%
Similar papers in this journal
Similar papers in this journal
- SMARTER-database: a tool to integrate SNP arraydatasets for sheep and goat breeds 94%
- NeuroVar: An Open-source Tool for Gene Expression and Variation Data Visualization for Biomarkers of Neurological Diseases 93%
- BatchEval Pipeline: Batch Effect Evaluation Workflow for Multiple Datasets Joint Analysis 92%
Similar papers in this journal
- Extensive In Silico Analysis of the Functional and Structural Consequences of SNPs in Human ARX Gene 95%
- Finding Consensus miRNAs Silencing KLF1 Expression as A Promising Therapeutic Option of Sickle Cell Anemia 92%
- Viral miRNAs Confer Survival in Host Cells by Targeting Apoptosis Related Host Genes 91%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.