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As a foundational step towards deciphering the phylogenetic structures of citrus genomes and the molecular bases of phenotypic variation, a reference whole genome sequence of a haploid derived from Clementine was produced and is currently being revised by the International Citrus Genome Consortium (ICGC) [ 13, 14].
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To detect variation, a reference-guided assembly was conducted by mapping the preprocessed raw SP3B sequence data to the H6 assembly via Bowtie2 v2.0.0-beta7 v2.0.0-beta7ameter) Samtools v0.1.18 andefaultf v3.3h (-minC 5 -minQ 20) identified sequence variation and classified typarameter variation by region of the aSamtools transcripts.
Furthermore, according to expression variation of a reference gene within a specific tissue, usually two to four reference genes are sufficient.
The laminar flame speeds were determined by determining the variation of a reference flame speed as a function of strain rate and computationally assisted non-linear extrapolations.
The genetic architecture of a trait is defined by the set of genes contributing to genetic variation within a reference population of genotypes together with information on their location in the genome and the effects of their alleles on traits, including intra-locus and inter-locus interactions, environmental dependencies, and pleiotropy.
The paired analysis method can reduce the measured variation in a reference sample design.
Comparative Genomic Hybridization (CGH) microarrays allow the detection of variation between a reference genome, whose sequences are targeted by the probes, and query genomes.
This program determines the pairwise variation of a reference gene with all other reference genes and defines the reference gene-stability measure M as the average pairwise variation of a particular gene with all other reference genes.
This comparative method uses a target assay for the DNA segment being interrogated for copy number variation and a reference assay for an internal control segment, which is normally a known single copy gene; moreover a reference sample is included.
Current computational methods for accurate alignment of these reads, including BWA and Bowtie2 are based on the Burrows-Wheeler Transform FM index, and they are designed to align short reads with minimal variation to a reference assembly.
The most stable reference genes were identified using the geNorm 3.5v (medgen.ugent.be/~jvdesomp/geNorm/) algorithm [ 59]. geNorm estimates an average expression stability value (M value) for each reference gene by the pairwise variation between a reference gene and all others reference genes tested.
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