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Reflections from heterogeneities within the sample are mapped as a function of thickness for any one position.
Scanning Hall probe microscopy (SHPM) is a novel scanned probe magnetic imaging technique whereby the stray fields at the surface of a sample are mapped with a sub-micron semiconductor heterostructure Hall probe.
This is because only a small fraction of reads in each ChIP-seq sample are mapped to heterozygote SNPs, and only these reads are informative for inferring allele-specificity.
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Trimmed reads from each sample were mapped to the Fragaria vesca genome v2.0.a1 (Fv2.0.a1
The quality-trimmed reads from each sample were mapped back onto the assembled contigs from that same sample using Bowtie (v0.12.9) with a 512 MB max best-first search frames value, Phred33 score quality setting, 21 base-pair seed length, and limit of 2 mismatches per seed.
By applying the kernel function, the sample is mapped linearly to the high-dimensional feature space.
The extent to which the X-rays are attenuated (absorbed or scattered) by the sample is mapped in three dimensions using a computer algorithm.
Firstly, DEGs indentified in each disease sample were mapped to PPI and TRI data.
Trimmed RNA reads from each sample were mapped back to this reference transcriptome using Bowtie2.
Each end of the paired-end reads for a sample was mapped separately.
More than 20 million reads per sample were mapped to the genome.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com