Pages that link to "Q30423375"
The following pages link to YAHA: fast and flexible long-read alignment with optimal breakpoint detection (Q30423375):
Displaying 31 items.
- LUMPY: a probabilistic framework for structural variant discovery. (Q21999523) (← links)
- Structural variation discovery in the cancer genome using next generation sequencing: computational solutions and perspectives (Q26991436) (← links)
- The Complete Genome Sequences, Unique Mutational Spectra, and Developmental Potency of Adult Neurons Revealed by Cloning (Q30277198) (← links)
- SAMBLASTER: fast duplicate marking and structural variant read extraction (Q30410889) (← links)
- Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms (Q30416550) (← links)
- Sprites: detection of deletions from sequencing data by re-aligning split reads (Q31041990) (← links)
- Structural variation detection using next-generation sequencing data: A comparative technical review. (Q31043037) (← links)
- Genome-wide detection of DNA double-stranded breaks induced by engineered nucleases. (Q35060760) (← links)
- PBHoney: identifying genomic variants via long-read discordance and interrupted mapping (Q35184957) (← links)
- A Long Fragment Aligner called ALFALFA. (Q35631053) (← links)
- Detecting DNA double-stranded breaks in mammalian genomes by linear amplification-mediated high-throughput genome-wide translocation sequencing (Q35975147) (← links)
- Orientation-specific joining of AID-initiated DNA breaks promotes antibody class switching. (Q36116985) (← links)
- Transient structural variations have strong effects on quantitative traits and reproductive isolation in fission yeast (Q36258476) (← links)
- BatAlign: an incremental method for accurate alignment of sequencing reads (Q36299119) (← links)
- Local sequence assembly reveals a high-resolution profile of somatic structural variations in 97 cancer genomes (Q36676741) (← links)
- DNA methylation profiles of diverse Brachypodium distachyon align with underlying genetic diversity (Q37383328) (← links)
- Population scale mapping of transposable element diversity reveals links to gene regulation and epigenomic variation (Q37515750) (← links)
- Diverse, Biologically Relevant, and Targetable Gene Rearrangements in Triple-Negative Breast Cancer and Other Malignancies (Q38768199) (← links)
- LAMSA: fast split read alignment with long approximate matches (Q39352297) (← links)
- BreakSeek: a breakpoint-based algorithm for full spectral range INDEL detection (Q42552455) (← links)
- Sequence analysis of European maize inbred line F2 provides new insights into molecular and chromosomal characteristics of presence/absence variants (Q48104068) (← links)
- A survey of localized sequence rearrangements in human DNA. (Q49616753) (← links)
- Heterogeneous rates of genome rearrangement contributed to the disparity of species richness in Ascomycota. (Q54955427) (← links)
- Human copy number variants are enriched in regions of low mappability (Q56894047) (← links)
- The Grayling Genome Reveals Selection on Gene Expression Regulation after Whole-Genome Duplication (Q57817108) (← links)
- Combining probabilistic alignments with read pair information improves accuracy of split-alignments (Q62496018) (← links)
- Phosphorylation at S2053 in Murine (S2056 in Human) DNA-PKcs Is Dispensable for Lymphocyte Development and Class Switch Recombination (Q64386916) (← links)
- A deletion in Eml1 leads to bilateral subcortical heterotopia in the tish rat (Q90367667) (← links)
- Kinase-dependent structural role of DNA-PKcs during immunoglobulin class switch recombination (Q90721989) (← links)
- CtIP is essential for early B cell proliferation and development in mice (Q92088877) (← links)
- Mapping and characterization of structural variation in 17,795 human genomes (Q95925271) (← links)