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Exact(10)
About half of the sequences (19 unigenes) matched to sequences of unknown function and without known protein domains.
Resulting sequences were matched to sequences in GENBANK via BLAST to determine the likely host species (98% sequence match).
More than 20 million 25-base 5'-end tags were obtained from untreated and 5Aza-treated cells and matched to sequences within the human genome.
19668 primer pairs matched to sequences from the genome browser.
The data were also matched to sequences from the H5N1 viral proteome.
Very few unigenes matched to sequences of nonvascular plants (bryophytes) or green algae.
Similar(50)
Hairpins were matched to sequence reads, using custom Perl scripts, allowing up to two mismatches per alignment.
TRFLP data was further matched to sequenced 16S rDNA amplicons from cultured bacteria to assist in assigning taxonomic identities (Additional file 4: Table S2).
Long (>15 nucleotide) primers match specifically with a designed target sequence, but they can also match to sequences that are complementary to shorter portions of the primer.
Only matches showing 100% identity over the complete CRISPR spacer sequences were retained, and matches to sequences found within CRISPR loci were ignored.
Genome similarity searches revealed sequence identity matches to sequence scaffolds on BTA6 for most unique ETS (91%).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com