Alignments of multiple genomes are a cornerstone of comparative genomics, but generating these alignments remains technically challenging and often impractical. We developed the msa_pipeline workflow (https://bitbucket.org/bucklerlab/msa_pipeline) to allow practical and sensitive multiple alignment of diverged plant genomes and calculation of conservation scores with minimal user inputs. As high repeat content and genomic divergence are substantial challenges in plant genome alignment, we also explored the effect of different masking approaches and parameters of the LAST aligner using genome assemblies of 33 grass species. Compared with conventional masking with RepeatMasker, a masking approach based on k-mers (nucleotide sequences of k len...
Multiple sequence alignments (MSAs) are used for structural1,2 and evolutionary predictions1,2, but ...
National audienceWhole genome alignment is a challenging problem in computational comparative genomi...
Schilbert H, Rempel A, Pucker B. Comparison of Read Mapping and Variant Calling Tools for the Analys...
Alignments of multiple genomes are a cornerstone of comparative genomics, but generating these align...
As the number of available genome sequences from both closely related species and individuals within...
Structural variants (SVs) are genetic sequence rearrangements that play a significant role in many c...
We present whole-genome assemblies of four divergent Arabidopsis thaliana strains that complement th...
Genome sequencing of closely related individuals has yielded valuable insights that link genome evol...
Genome resequencing with short reads generally relies on alignments against a single reference. Geno...
The 1001 Genomes Project generated a polymorphism (SNP) and short structural variant (short SV) map ...
Discovery of the DNA double helix represents one of the great milestones in biology. For plant resea...
Genome sequencing of closely related individuals has yielded valuable insights that link genome evol...
We have sequenced the genomes of 18 inbred accessions of Arabidopsis thaliana at ~40x coverage using...
Using next-generation sequencing technologies it is possible to resequence entire plant genomes or s...
Multiple sequence alignment (MSA) is the heart of comparative sequence analysis. Recent studies demo...
Multiple sequence alignments (MSAs) are used for structural1,2 and evolutionary predictions1,2, but ...
National audienceWhole genome alignment is a challenging problem in computational comparative genomi...
Schilbert H, Rempel A, Pucker B. Comparison of Read Mapping and Variant Calling Tools for the Analys...
Alignments of multiple genomes are a cornerstone of comparative genomics, but generating these align...
As the number of available genome sequences from both closely related species and individuals within...
Structural variants (SVs) are genetic sequence rearrangements that play a significant role in many c...
We present whole-genome assemblies of four divergent Arabidopsis thaliana strains that complement th...
Genome sequencing of closely related individuals has yielded valuable insights that link genome evol...
Genome resequencing with short reads generally relies on alignments against a single reference. Geno...
The 1001 Genomes Project generated a polymorphism (SNP) and short structural variant (short SV) map ...
Discovery of the DNA double helix represents one of the great milestones in biology. For plant resea...
Genome sequencing of closely related individuals has yielded valuable insights that link genome evol...
We have sequenced the genomes of 18 inbred accessions of Arabidopsis thaliana at ~40x coverage using...
Using next-generation sequencing technologies it is possible to resequence entire plant genomes or s...
Multiple sequence alignment (MSA) is the heart of comparative sequence analysis. Recent studies demo...
Multiple sequence alignments (MSAs) are used for structural1,2 and evolutionary predictions1,2, but ...
National audienceWhole genome alignment is a challenging problem in computational comparative genomi...
Schilbert H, Rempel A, Pucker B. Comparison of Read Mapping and Variant Calling Tools for the Analys...