Sentences with phrase «nucleotide sequence data»

1981 - The EMBL Data Library is founded — the first central depository of nucleotide sequence data in the world (precursor to EMBL - EBI).

Not exact matches

However, based on data now available, we see that the sequence of the 3 billion nucleotides in any individual genome is unique in comparison with the sequence of another individual's genome, while the degree of sequence similarity between the 3 billion nucleotides in any two genomes is remarkably high.

The sequencing data generated in this study for CGG10022 and CGG10023 are available from the European Nucleotide Archive, using accession no.

Data deposition: Sequence data generated for this study (samples CGG10022 and CGG10023) have been deposited in the European Nucleotide Archive (accessionData deposition: Sequence data generated for this study (samples CGG10022 and CGG10023) have been deposited in the European Nucleotide Archive (accessiondata generated for this study (samples CGG10022 and CGG10023) have been deposited in the European Nucleotide Archive (accession no.

Here we explore the power of two haplotype - based statistics — the integrated haplotype score (iHS) and the Derived Intra-allelic Nucleotide Diversity (DIND) test — in the context of next - generation sequencing data, and evaluate their robustness to demography and other selection modes.

However, the NextSeq series ™ NGS generates genome - wide sequence data as «digital data» in the resolution of single nucleotide and has no specificity, discrimination and sensitivity issues.

The resulting consensus sequences averaged 16,231 ± 455 bp, or 98.1 % of the complete mitochondrial genome, with the average number of reads per nucleotide position (fold - sequence coverage) ranging from 7.4 × to 117 × among the 9 individuals (Supplementary Data 1).

The sequence data easily can be used to identify single nucleotide deletion, insertion, polymorphism and translocation and copy a number of changes on the DNA level.

In turn, Genbank will distribute the sequence data to the European Molecular Biology Laboratory's Nucleotide Sequence Database, EMBL - Bank [ebi.ac.uk], and the DNA Data Bank of Japan, DDBJ [ddbj.nigsequence data to the European Molecular Biology Laboratory's Nucleotide Sequence Database, EMBL - Bank [ebi.ac.uk], and the DNA Data Bank of Japan, DDBJ [ddbj.nig.ac.data to the European Molecular Biology Laboratory's Nucleotide Sequence Database, EMBL - Bank [ebi.ac.uk], and the DNA Data Bank of Japan, DDBJ [ddbj.nigSequence Database, EMBL - Bank [ebi.ac.uk], and the DNA Data Bank of Japan, DDBJ [ddbj.nig.ac.Data Bank of Japan, DDBJ [ddbj.nig.ac.jp].

Microsatellite genotypes were obtained for 203 clinical infection samples from eight locations, and Illumina paired - end sequences were obtained to yield high coverage genome - wide single nucleotide polymorphism (SNP) data for 65 clinical infection samples from four locations.

By SNP analysis, single nucleotide differences between the sequences of 22Rv1 - associated XMRV and XMRV genomes detected in prostate cancer tissues [VP35, VP42, and VP62 (2006)-RSB-(red lollipops) are corrected by the deep sequencing coverage data (black lollipops).

To ensure that sequence data are freely available, scientific journals require that new nucleotide sequences be deposited in a publicly accessible database as a condition for publication of an article.

For example, an advisory committee made up of members of the European Molecular Biology Laboratory Nucleotide Sequence Database (EMBL - Bank) in the United Kingdom, the DNA Data Bank of Japan (DDBJ), and GenBank of the National Center for Biotechnology Information (NCBI) in the United States oversees the International Nucleotide Sequence Database Collaboration (INSDC).