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Abbreviation : PSVs
Long Form : paralogous sequence variants
No. Year Title Co-occurring Abbreviation
2018 A New Single Nucleotide Polymorphism Database for Rainbow Trout Generated Through Whole Genome Resequencing. MSVs, RAD, RRL, SNPs, WSU
2018 PMERGE: Computational filtering of paralogous sequences from RAD-seq data. RAD-seq, SNPs
2017 A SNP Based Linkage Map of the Arctic Charr (Salvelinus alpinus) Genome Provides Insights into the Diploidization Process After Whole Genome Duplication. ---
2014 A resource of single-nucleotide polymorphisms for rainbow trout generated by restriction-site associated DNA sequencing of doubled haploids. DH, MAF, RAD, SNP
2013 Recombination dynamics of a human Y-chromosomal palindrome: rapid GC-biased gene conversion, multi-kilobase conversion tracts, and rare inversions. MSY
2011 A dense SNP-based linkage map for Atlantic salmon (Salmo salar) reveals extended chromosome homeologies and striking differences in sex-specific recombination patterns. MSVs, SNPs, WGD
2009 High-throughput haplotype determination over long distances by haplotype fusion PCR and ligation haplotyping. HF-PCR, SNPs
2004 Duplications of the Y-chromosome specific loci P25 and 92R7 and forensic implications. SNPs
2002 Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome. LCRs, NCBI, NF1, SNPs