Sentence examples similar to by genome sequence map from inspiring English sources

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We verified the consistency of the chromosome whole assembly by comparing the genome sequence map with a genetic experimental map obtained by conjugation [22].

Location of the insert and intactness of other parts of the genome of the mutant was verified by genome sequencing and mapping to the reference genome of HAMBI 540T.

Gene replacement deletion mutants were constructed also for nifQ in both HAMBI 540T and HAMBI 1141, and the mutant strains (HAMBI 3479 and HAMBI 3481 respectively) verified by genome sequencing and mapping to the respective reference strains.

We analyzed travel-associated clinical isolates of Escherichia coli O104:H4, including 1 from the 2011 German outbreak and 1 from a patient who returned from the Philippines in 2010, by genome sequencing and optical mapping.

Assuming that the physical length of these genomic intervals is correctly predicted by the genome sequence, the map length divided by the segment size yields a recombination rate (cM/Mb) point estimate for each scaffold.

A total of 73 out 115 microsatellites marker were found to align on the porcine genome sequence assembly map position by BLAST analysis.

The EST assemblies and cDNA clones were used in similarity analyses after interspersed repetitive sequences and low-complexity regions (such as polynucleotides and microsatellites) had been masked with the RepeatMasker program [ 56]. EST assemblies and cDNA clones on the pig genome sequence were mapped by using a BLAST similarity search [ 23] with the latest pig genome sequence, Sscrofa10.2 [ 6].

Intriguingly, this emu sequence mapped with high confidence to the chicken Z chromosome as predicted by the genome sequence and genetic and physical maps [ 47].

These inferred relationships are not an artifact of generating the wMelCS consensus genome sequences by mapping to the wMel genome: The same patterns of relatedness are observed when wMelCS reads are mapped to the wMelPop assembly for the purposes of variant calling.

Identification of variants is straightforward for isolate genome sequencing by mapping all reads to a reference genome.

We then determined the validity of using the tiling microarray data to predict gene presence or absence by comparing mapping data with genome sequence data using the two genome sequenced strains, P1/7 and 89-1591 anderiveded a PPC value to determine the presence or absence of a gene.

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