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However, further studies are needed to understand the 'logic' of long-range interactions, and massively parallel analyses such as TRIP 119 are paving the way in this direction.
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In this paper, we describe the characterization of STAT6 target genes in Ramos and BEAS2B cells using various types of massively parallel sequencing analyses.
Massively parallel sequencing analyses have revealed a common mutation within the MYD88 gene (MYD88L265P) occurring at high frequencies in many non-Hodgkin lymphomas (NHLs) including the rare lymphoplasmacytic lymphoma, Waldenström's macroglobulinemia (WM).
Thus, massively parallel genetic expression analyses of vertebrate diapause via NGS-based RNA-Seq are unavailable for comparison with the current study.
We used whole exome capture and massively parallel sequencing to analyse a large family with 46,XY DSD and 46,XX premature ovarian insufficiency.
Previously published Massively Parallel Signature Sequencing (MPSS) analyses of hESC gene expression [30] [32] were examined to determine whether the SPIE receptors are expressed in hESC.
The Medical Genetics Laboratories of the department offer extensive fee-based genetic tests including the use of massively parallel sequencing for molecular analyses of retinal diseases.
To test this, we used massively parallel Illumina sequencing to analyse small RNAs from auditory forebrain of adult zebra finches exposed to tape-recorded birdsong or silence.
In conclusion, we report for the first time an integrated genomic picture of the quadrupleWT GIST, using massively parallel sequencing and gene expression analyses, and have identified a unique subset of GIST among the family of the KIT/PDGFRA WT GIST [ 60].
We report for the first time an integrated genomic picture of KITWT/ PDGFRAWT/ SDHWT/ RAS-PWT GIST, using massively parallel sequencing and gene expression analyses, and found that quadrupleWT GIST have an expression signature that is distinct from SDH-mutant GIST as well as GIST harbouring mutations in KIT or PDGFRA.
Moreover, in our previous studies (13 15), we showed that more accurate analyses (i.e. absolute CNV calling) are feasible by using combined analyses, such as massively parallel sequencing with high-resolution comparative genomic hybridization (CGH) array (14, 15).
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