Leggermente farfalla moda haplotype based variant detection from short read sequencing Orfano Ritiro sforzo
Computational methods for chromosome-scale haplotype reconstruction | Genome Biology | Full Text
Variant calling: Considerations, practices, and developments - Zverinova - 2022 - Human Mutation - Wiley Online Library
Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications | Nature Genetics
Frontiers | Long-Read Sequencing Emerging in Medical Genetics
Long walk to genomics: History and current approaches to genome sequencing and assembly - ScienceDirect
PDF] Haplotype-based variant detection from short-read sequencing | Semantic Scholar
Haplotype-based variant detection from short-read sequencing
HAPDeNovo: a haplotype-based approach for filtering and phasing de novo mutations in linked read sequencing data | BMC Genomics | Full Text
Genes | Free Full-Text | Inferring Signatures of Positive Selection in Whole-Genome Sequencing Data: An Overview of Haplotype-Based Methods
Sequencing 101: ploidy, haplotypes, and phasing — how to get more from your sequencing data - PacBio
Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis | Scientific Reports
Variant calling with Freebayes | In-depth-NGS-Data-Analysis-Course
IJMS | Free Full-Text | Long-Read Sequencing Improves the Detection of Structural Variations Impacting Complex Non-Coding Elements of the Genome
A complete reference genome improves analysis of human genetic variation | Science
Haplotype-based variant detection from short-read sequencing
PDF] Haplotype-based variant detection from short-read sequencing | Semantic Scholar
Increasing calling accuracy, coverage, and read-depth in sequence data by the use of haplotype blocks | PLOS Genetics
Single nucleotide variants| Oxford Nanopore Technologies
Sequencing 101: ploidy, haplotypes, and phasing — how to get more from your sequencing data - PacBio
NanoCaller for accurate detection of SNPs and indels in difficult-to-map regions from long-read sequencing by haplotype-aware deep neural networks | Genome Biology | Full Text
PDF] Haplotype-based variant detection from short-read sequencing | Semantic Scholar
Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing | Nature Communications
A unified haplotype-based method for accurate and comprehensive variant calling | Nature Biotechnology
Benchmarking challenging small variants with linked and long reads - ScienceDirect
PDF] Haplotype-based variant detection from short-read sequencing | Semantic Scholar