Publication date
January 2016
DOIAbstract
With this new version, you are no longer forced to use the haplotype approach to filter the markers. The SNP approach is available with the functions: filter_maf, filter_fis and filter_het
With this new version, you are no longer forced to use the haplotype approach to filter the markers. The SNP approach is available with the functions: filter_maf, filter_fis and filter_het
Script to remove SNPs only polymorphic relative to the genome. This was used to remove SNPs when ali...
AbstractIn the Human Genome Project, the most common type of these variations is single nucleotide p...
This R script creates a whitelist to input into STACKS v. 1.35, by eliminating SNPs from the last bp...
<p>Each step of the filtering process and the number of SNPs remaining are shown in sequence. Putati...
v.0.4.6 I'm pleased to announce that stackr parallel mode now works with Windows! Nothing to instal...
<p>Upper panel shows results from single-SNP analysis; lower panel presents results of haplotype-bas...
High-throughput next-generation sequence-based genotyping and single nucleotide polymorphism (SNP) d...
Here we present SNP-SCALE, a new single nucleotide polymorphism genotyping protocol based on allele-...
AbstractThis paper proposes a new framework for the selection of tag SNPs based on haplotypes instea...
v.0.4.5 temporary fix to tidy_genomic_data to read unconventional Tassel VCF new function ibdg_fh ...
Summary: The search for the association between complex disea-ses and single nucleotide polymorphism...
Single nucleotide polymorphisms (SNPs) play a central role in the identification of susceptibility g...
Abstract Background There is recently great interest in haplotype block structure and haplotype tagg...
This release corresponds to the updated documentation and functionalities requested by reviewers of ...
When we sequence a diploid individual, the output actually comprises two genomes: one from the pater...
Script to remove SNPs only polymorphic relative to the genome. This was used to remove SNPs when ali...
AbstractIn the Human Genome Project, the most common type of these variations is single nucleotide p...
This R script creates a whitelist to input into STACKS v. 1.35, by eliminating SNPs from the last bp...
<p>Each step of the filtering process and the number of SNPs remaining are shown in sequence. Putati...
v.0.4.6 I'm pleased to announce that stackr parallel mode now works with Windows! Nothing to instal...
<p>Upper panel shows results from single-SNP analysis; lower panel presents results of haplotype-bas...
High-throughput next-generation sequence-based genotyping and single nucleotide polymorphism (SNP) d...
Here we present SNP-SCALE, a new single nucleotide polymorphism genotyping protocol based on allele-...
AbstractThis paper proposes a new framework for the selection of tag SNPs based on haplotypes instea...
v.0.4.5 temporary fix to tidy_genomic_data to read unconventional Tassel VCF new function ibdg_fh ...
Summary: The search for the association between complex disea-ses and single nucleotide polymorphism...
Single nucleotide polymorphisms (SNPs) play a central role in the identification of susceptibility g...
Abstract Background There is recently great interest in haplotype block structure and haplotype tagg...
This release corresponds to the updated documentation and functionalities requested by reviewers of ...
When we sequence a diploid individual, the output actually comprises two genomes: one from the pater...
Script to remove SNPs only polymorphic relative to the genome. This was used to remove SNPs when ali...
AbstractIn the Human Genome Project, the most common type of these variations is single nucleotide p...
This R script creates a whitelist to input into STACKS v. 1.35, by eliminating SNPs from the last bp...
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