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In conclusion, when the next round of ENIGMA studies has been completed, there will be a scaffolding of credible genetic variants on which to build and test new models of macroscale brain development, the implications of those variants for neuropsychiatric disease, and a new basis to probe the genetic architecture of the living human brain.
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We observed an excess of rare, derived NR2E1 variants, as indicated by the significantly negative Fu and Li's D* and F* values, which could be evidence of a 'selective sweep' (i.e. the rare variants have 'hitch-hiked' along with a variant on which positive selection has occurred) (Fay & Wu 2000).
There are two application processor modules available for the current version: one from Marvell and one based on Nvidia's K1 (variants of which power the Shield tablet and the Nexus 9).
Following this, we formulate several candidate techniques for computing comparison genomes, several variants of which are based on LP.
The most common management alteration was the addition of image guidance based on anatomic variants on MRI, which occurred in 81 patients (35.0%).
The ability to look with increased resolution at the non-coding space of the genome has recently encouraged an increasing number of laboratories to investigate the impact of cis-regulatory-associated variants on disease, which as a result has motivated the development of bioinformatics tools for linking variants with regulatory elements.
Epistasis is the phenomenon whereby the phenotypic effect of variation in one gene depends on which variants of other genes are present [ 16].
Notably, this pattern is reversed when we focus only on those variants for which the minor alleles are ancestral.
This study was focused on the variants for which existing data were contradictory and we went into detail by also performing analyses stratified for ACPA.
Based upon the simulation results as shown in Table 3, the power achieved using these two types of methods, haplotype-based pedigree tests vs. rare variants based pedigree tests, depending on which one had greater contribution on disease between haplotypes and rare variants.
To date, much of the focus has been on rare protein-coding variants, for which potential impact can be estimated from the genetic code, but determining the impact of rare noncoding variants has been more challenging.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com