Searching journal content for articles similar to Ferdig et al. 8 (1): 41.

Displaying results 1-10 of 5635
For checked items
  1. ...), NPC lines, and developmental timepoints, to generate a list of putative enhancer regions to investigate using the phNPC model. Whereas other enhancer mapping tools such as massively parallel reporter assays (MPRAs) have been used to identify putative enhancer regions in primary human cortical cells...
  2. ...were functionally annotated by mapping them to in-house profiles of the Clusters of Orthologous Genes (COG) database (2020 release) (Galperin et al. 2021) with HMMER v3.1b2 (e-value < 0.001; http://hmmer.org). The 26 major prokaryotic functional categories defined in the COG database were assigned...
  3. ...are indeed proximal in physical space and vice versa. A CTG distance matrix is constructed based on the similarity of the diffusion property between genomic loci in the Hi-C contact map. Except for self-distance, the calculation of CTG distance (L1 distance between rows of transition probability matrix...
  4. ...and mappingFrom our four independent replicates for the 11 time points of prebloodmeal and PBM, Illumina NovaSeq 6000 paired-end sequencing generated 1,160,607,602 fragment pairs (2,321,215,204 reads). We obtained a mean of 26,377,445.5 fragments per sample (ranging from 19,503,828 to 34,008,005 fragments...
  5. ...A chromosome-scale epigenetic map of the Hydra reveals conserved regulators of cell state Jack F. Cazet1, Stefan Siebert1,2, Hannah Morris Little1, Philip Bertemes3, Abby S. Primack1, Peter Ladurner3, Matthias Achrainer3, Mark T. Fredriksen4, R. Travis Moreland4, Sumeeta Singh4, Suiyuan Zhang4...
  6. ...and chimpanzee cerebral organoids, indicating that cell-type composition can be accurately matched between closely related primate species and expression differences within each type identified (Mora-Bermúdez et al. 2016; Kanton et al. 2019; Pollen et al. 2019).Here, we report transcriptome maps of the human...
  7. ...to single nucleotide polymorphisms (SNPs) can impact gene function by altering exonic sequence or by changing gene regulation. Recent studies estimate that 93% of disease-associated variants are in noncoding DNA (Welter et al. 2014) and 60% of causal variants map to regulatory elements (Farh et al. 2015...
  8. ...variants and their mechanisms of action in relevant biological systems at scale. The identification of functional variants relative to proxy variants in high linkage disequilibrium (LD) presents an additional challenge. Recent studies have begun to map molecular quantitative trait loci (molQTLs) for gene...
  9. ...and quantitative metabolic variationTo gain deeper insight into the regulation of plant metabolism within the epiRIL population, QTLepi analysis was performed on all metabolites using a genetic map based on differentially methylated regions as physical markers (Colome-Tatche et al. 2012). To verify that these DMRs...
  10. ...ones. Sequencing metrics and coverage The use of target enrichment technology followed by multiplexed Illumina sequencing allowed obtaining an average of 4.35 million 75-bp reads per sample (Supplemental Table 1). Filtering them according to read pairing, sequence quality, and mapping quality Faucon et...
For checked items

Preprint Server