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  1. ...but substantial amounts of total RNA (Supplemental Table 1). Subsequently, the extracted and purified RNA fragments were prepared for high-throughput sequencing using a cDNA library protocol tailored for short RNA transcripts. The library size distribution indicated a successful extraction and library preparation...
  2. ..., two reference colugo mtDNA s and six published partial mitochondrial rRNA sequences from individuals from Peninsular Malaysia (GVA 1–3) andWest Java (GVA 4–6) ( Janečka et al. 2008). Enforcing different read depth thresholds for inclusion of a site in the alignment (e.g., read depth 53–253) had...
  3. ...Mature miRNA 650 Population genomics of rhesus macaques Genome Research 1655 www..org but more similar between species than the counts of synonymous variants (7810.1 in rhesus versus 6551.7 in humans; t-test P = 7.66 × 10−47) (see also Yuan et al. 2012). Consequently, the ratio of nonsynonymous...
  4. ...lost, on the chimpanzee Y (Fig. 3; Hughes et al. 2010). We assembled the RNA-seq data from gorilla testis (Supplemental Table S9) and used various filtering strategies and additional gorilla and human data to reconstruct the gorilla Y-Chromosome genes (Methods; Supplemental File S1). This was performed...
  5. .... Here, we report a large-scale study of the expression evolution of DNA-based functional gene duplicates in three major mammalian lineages (placental mammals, marsupials, egg-laying monotremes) and birds, on the basis of RNA sequencing (RNA-seq) data from nine species and eight organs. We observe...
  6. ...is the only other primate curated to this degree of detail for chromosomal accuracy. To annotate the vervet for gene content, we utilized the collective methods deployed at NCBI (http://www.ncbi.nlm. nih.gov//annotation_euk/process/), taking as input RNA sequencing (RNA-seq) data from total RNA and small RNA...
  7. ...et al. 2000). If the transduced sequence contains an exon, it may be inserted near existing exons, resulting in an exon shuffling event. Assuming RNA pol II transcription and normal post-transcriptional processing, two ormore exons in the transduced sequencemay bemerged and reinserted, resulting...
  8. ...region indicated with dashed rectangles in the upper plot. MHC-I, MHC-II and APG are marked and labeled individually, with the width of rectangles corresponding to gene lengths. Maximum relative expression: the maximum fraction of total MHC-I expression (FPKM) attributable to a sequence across all RNA...
  9. ...blot analysis ( LAMP1, AKAP2 , and SPTLC1 ) ( Fig. 2C ; Suppl. Fig. 1) were caused by sequence differences between African great ape transcripts and the probes in the microarray (Suppl. Table 1). This is not unexpected, as mismatches between African great ape RNA samples and oligonucleotide probes...
  10. ..., there are several caveats. For example, microarrays based on human oligonucleotide sequences may not accurately detect levels of expression in nonhuman primates nor detect significant alternative splicing of mRNAs ( Modrek and Lee 2002 ; Hsieh et al. 2003 ; Preuss et al. 2004 ; Steinmetz and Davis 2004...
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