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  1. ...Xinyang Yu1 and Michael J. Buck1,2 1New York State Center of Excellence in Bioinformatics and Life Sciences and Department of Biochemistry, State University of New York at Buffalo, Buffalo, New York 14203, USA; 2Department of Biomedical Informatics, State University of New York at Buffalo, Buffalo...
  2. ...PowerBLAST: A New Network BLAST Application for Interactive or Automated Sequence Analysis and Annotation Jinghui Zhang 1 and Thomas L. Madden National Center for Biotechnology Information (NCBI), National Library of Medicine, National Institutes of Health...
  3. ...classified genes according to intact start and stop codons, low-quality annotation, and partial annotation. Also, for each gene, a representative transcript was chosen based on reciprocal best hit BLAST results with protein sequences of human representative transcripts. For genes with no reciprocal best hit...
  4. ...in the assembly of each isolate using BLAST. The results were manually curated, and multiple protein alignments were generated. The presence and distribution pattern of amino acid substitutions were investigated manually.Data accessThe raw sequence data generated in this study have been submitted to the NCBI Bio...
  5. ...) (Vacic et al. 2007). The canonical structure of FZNF genes resembles that of KZNFs, with the FiNZ domain being encoded by a single exon upstream of a second exon consisting of an array of ZNF domains (Imbeault et al. 2017).We reannotated putative FZNF genes using a combination of BLAST (Altschul et al...
  6. ...× 10−6. Protein structure similarity was explored using I-TASSER (Roy et al. 2010) as in Ansell et al. (2019) and Supplemental Methods. Blast2GO (Conesa et al. 2005) version 4.1.9 was used to assign Enzyme Code (EC) and Gene Ontology (GO) terms. We compared the existing protein product names to the new...
  7. ...-based methods capture transcripts in an unbiased manner and are capable of whole transcriptome coverage. For example, laser capture microdissection physically separates cells and structures of interest within a tissue, which can then be profiled by a variety of methods including RNA-seq (Emmert-Buck et al. 1996...
  8. ...unique cyclocontigs in the ISOLATES data set reconstructed by plasmidSPAdes+ (A) and the Venn diagram for cyclocontigs identified as plasmids by plasmidVerify, cyclocontigs identified as plasmids by BLAST (span >10%), and cyclocontigs containing ARGs (B). (A) Each dot represents a cyclocontig reported...
  9. ...al. 2006; Buck et al. 2010).A paralog of nebulin is the nebulin-related anchoring protein (Nrap) (Luo et al. 1997). Nrap is the second largest (∼196 kDa) member of the nebulin family of proteins (Luo et al. 1997; Pappas et al. 2011). It is a scaffolding protein, with roles in myofibrillar assembly...
  10. ...ready cell generation, nontargeting, and HIV-1 targeting guides 5 For CRISPRi cell lines, Jurkat clones were transduced with pseudotyped lentiviruses encoding Lenti-6 dCas9-KRAB-blast (Addgene #89567) by spinoculation. Two days post-transduction, 8 μg/mL blasticidin was 7 added to the culture medium...
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