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Our procedure is implemented as CotQuest, a suite of scripts designed for use with the statistics package SAS.
CASAVA1.8 is a suite of scripts including sequence alignment of the complete genome (build37), counting and detection of allelic variants (SNPs and Indels).
For this goal, we developed a suite of scripts that allows users to customize these analyses by modifying the minimal GI length, or the similarity cut-off sequence (i.e., the genomic Core Island of each genome with a certain genomic compositional dissimilarity).
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This script to track lava level is one of a suite of Matlab scripts that comprise the thermal camera image acquisition scheme described by Patrick et al. (2014).
The promoter sequences of L1 elements from L1Xplorer or the UCSC genome database were extracted using a suite of Perl scripts that detect and extract the core L1 promoter sequences by performing BLAST searches.
Data were collected using a suite of Perl scripts (available from the authors on request), accessing Ensembl and Vega via the Perl API (Bio::EnsEMBL) and other sources (dbSNP and HapMap) via an automated user script to access each relevant website, to construct a database using MySQL (software version MySQL 5.0.67-0ubuntu6).
All small RNA data were processed by a suite of perl scripts.
ACT is available as a suite of downloadable scripts corresponding to the aggregation, correlation and saturation components of the toolbox.
Haploscribe is a suite of software scripts that phase whole-genome data across entire chromosomes by genetic analysis [ 8].
A suite of custom scripts was designed to evaluate the quality of the resultant RNA-Seq data.
We have developed a mapping strategy and a suite of software scripts to update the chromosomal positions of oligomer sequences used for SNP genotyping on high density arrays.
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CEO of Professional Science Editing for Scientists @ prosciediting.com