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Data from: Geographically-stratified HIV-1 group M pol subtype and circulating recombinant form sequences
负责人:
关键词:
HIV-1;GenBank Search;molecular epidemiology;Subtyping;pol Sequences
DOI:
doi:10.5061/dryad.56j2n
摘要:
sequences that represent HIV-1 group M sequence diversity. Representative pol sequences differ from representative complete genome sequences because not al
Data from: Two low coverage bird genomes and a comparison of reference-guided versus de novo genome assemblies
负责人:
关键词:
Genome;Nucifraga columbiana;Centrocercus minimus;Mitochondria;Clark's Nutcracker;Gunnison Sage-Grouse;low coverage genome sequencing;de novo Assembly;chromosome annotation;reference-guided assembly
DOI:
doi:10.5061/dryad.qn1n2
摘要:
ng assemblies. Our results demonstrate that even lower-coverage genome sequencing projects are capable of producing informative and useful genomic resources, par
Data from: De novo assembly of a chromosome-level reference genome of red spotted grouper (Epinephelus akaara) using nanopore sequencing and Hi-C
负责人:
关键词:
Genomics\/Proteomics;Transcriptomics;nanopore sequencing;Epinephelus akaara;Fish;Red Spotted Grouper (Epinephelus akaara);Red Spotted Grouper
DOI:
doi:10.5061/dryad.4398b9f
摘要:
. The genome contained 43.02% repeat sequences and 5,480 non-coding RNAs. Furthermore, after mining several RNA-seq datasets, 23,809 (99.5%) genes wer
Mouse lemur reference genome and diversity panel.
负责人:
BGI
关键词:
Genome sequencing and assembly Multiisolate
DOI:
doi:10.26036/cnphis0001816
摘要:
nerate whole genome sequences from additional mouse lemurs, both to identify DNA sequence variation within Microcebus murinus and to characterize genomic differences amo
Data from: De novo genome assembly of Camptotheca acuminata, a natural source of the anti-cancer compound camptothecin
负责人:
关键词:
DOI:
doi:10.5061/dryad.nc8qr
摘要:
ntation of the genome sequence including genic regions. Using a novel genome annotation method, we annotated 31 825 genes encoding 40 332 gene models. Based on sequence
Data from: De novo sequencing and variant calling with nanopores using PoreSeq
负责人:
关键词:
nanopore sequencing;variant calling;error correction
DOI:
doi:10.5061/dryad.84d4j
摘要:
The accuracy of sequencing single DNA molecules with nanopores is continually improving, but de novo genome sequencing and assembly usi

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