Searching journal content for articles similar to Sakate et al. 13 (5): 1022.

Displaying results 1-10 of 177
For checked items
  1. ...wild isolate VSL2202 and ZF1220 compared with C. briggsae strains. (E) Heatmap showing cDNA sequence identity of Cni-shls-1 (top), Cni-otub-3 (middle), and Cni-neib-1 (bottom) across all C. nigoni strains. Note that Cni-neib-1 sequences are 100% identical across all strains. (F) Gene models flanking...
  2. .... This has made it difficult to distinguish genes that are expressed and potentially functional from pseudogenes. To address this limitation, we sequenced HiFi, full-length nonchimeric (FLNC) cDNA using a PacBio isoform sequencing (Iso-Seq) assay (Methods) (Dougherty et al. 2018). We generated or analyzed...
  3. ...for which the chimpanzee DNA sequence is known, 207 are more highly expressed in humans and 199 in chimpanzees. Thus, although the up-regulation of genes on the human lineage may be real, further work is needed to verify it. This might be done using cDNA arrays that are less sensitive to DNA sequence...
  4. ...-specific evolution because of their potential for dramatic and irreversible mutation. The low-quality nature of the current chimpanzee genome assembly precludes the reliable identification of many of these differences. To circumvent this, we applied a method to optimally map chimpanzee fosmid paired-end sequences...
  5. ...of 366 sequences obtained by RELA ChIP in HeLa cells combined with the analysis of ENCODE RELA ChIP-seq (26-bp single-end data) from the lymphoblast cell line GM12878 and led to the conclusion that ∼11% of NF-kB-bound regions contain an Alu-derived NF-kB motif (Antonaki et al. 2011). Although our study...
  6. ...not contain a gene annotation and was not an EST entry, Genscan ( Burge and Karlin 1997 ) was applied to the human sequence starting 50 kb before and ending 50 kb after the alignment to the chimpanzee cDNA contig. Identified coding regions were extracted and collected in a local database, which was again...
  7. ...characterize these complex regions to gain insight into the impact of genomic diversity on health and disease. Here we resolve the organization of complete major histocompatibility complex (MHC) class II regions in rhesus macaques by using a long-read sequencing strategy (Oxford Nanopore Technologies...
  8. ...(Chambers et al. 2009; Ohnuki et al. 2014).To generate RNA-seq data, we used three clones of three human individuals and four clones of two cynomolgus macaque individuals. After 5 days of differentiation, the cells showed characteristics of neural progenitors and were harvested at days 5, 7, and 9. cDNA...
  9. ...), partial coverage genomic arrays ( Locke et al. 2003 ), cDNA arrays ( Fortna et al. 2004 ), end-sequence profiling ( Newman et al. 2005 ), draft sequence ( Chimpanzee Sequencing and Analysis Consortium 2005 ), and high-quality sequence from chimp Chromosome 21 (orthologous to human Chromosome 22...
  10. .... RNA isolation and cDNA preparation Cytoplasmic RNA was isolated from lymphoblastoid and fibroblast cell cultures derived from three chimpanzees and four humans, as well as lymphoblastoid cells from one bonobo, one gorilla, one orangutan, and one macaque, using the RNeasy kit (Qiagen). First strand cDNA...
For checked items

Preprint Server