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Academic Journal

Evaluation of vicinity-based hidden Markov models for genotype imputation.

Subjects: *HIDDEN Markov models; *NUCLEOTIDE sequencing; *MOSAICISM

  • Source: BMC Bioinformatics. 8/29/2022, Vol. 23 Issue 1, p1-26. 26p.

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Academic Journal

Accuracy benchmark of the GeneMind GenoLab M sequencing platform for WGS and WES analysis.

Subjects: *NUCLEOTIDE sequencing; *LIFE sciences

  • Source: BMC Genomics. 7/25/2022, Vol. 23 Issue 1, p1-11. 11p.

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Academic Journal

Binning long reads in metagenomics datasets using composition and coverage information.

Subjects: *METAGENOMICS; *NUCLEOTIDE sequencing; *ERROR rates

  • Source: Algorithms for Molecular Biology. 7/11/2022, Vol. 17 Issue 1, p1-15. 15p.

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Academic Journal

Genome sequences of 38 Fusarium oxysporum strains.

Subjects: *FUSARIUM oxysporum; *NUCLEOTIDE sequencing; *CULTIVARS

  • Source: BMC Research Notes. 6/27/2022, Vol. 15 Issue 1, p1-5. 5p.

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Academic Journal

ACO:lossless quality score compression based on adaptive coding order.

Subjects: *NUCLEOTIDE sequencing; *VIDEO coding; *WHOLE genome sequencingCHINA

  • Source: BMC Bioinformatics. 6/7/2022, Vol. 23 Issue 1, p1-14. 14p.

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Academic Journal

Inter-assay variability of next-generation sequencing-based gene panels.

Subjects: *NUCLEOTIDE sequencing; *GENE frequency; *GENES

  • Source: BMC Medical Genomics. 4/15/2022, Vol. 15 Issue 1, p1-11. 11p.

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Academic Journal

3GOLD: optimized Levenshtein distance for clustering third-generation sequencing data.

Subjects: *NUCLEOTIDE sequencing; *ERROR rates; *CENTROID

  • Source: BMC Bioinformatics. 3/20/2022, Vol. 23 Issue 1, p1-18. 18p.

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Academic Journal

Mini-XT, a miniaturized tagmentation-based protocol for efficient sequencing of SARS-CoV-2.

Subjects: *GENE libraries; *NUCLEOTIDE sequencing; *WHOLE genome sequencing

  • Source: Journal of Translational Medicine. 3/3/2022, Vol. 20 Issue 1, p1-11. 11p.

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Academic Journal

A guide for the diagnosis of rare and undiagnosed disease: beyond the exome.

Subjects: *RARE diseases; *NUCLEOTIDE sequencing; *SYMPTOMS

  • Source: Genome Medicine. 2/28/2022, Vol. 14 Issue 1, p1-22. 22p.

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Academic Journal

Rare disorders have many faces: in silico characterization of rare disorder spectrum.

Subjects: *HUMAN phenotype; *NUCLEOTIDE sequencing; *RARE diseases

  • Source: Orphanet Journal of Rare Diseases. 2/22/2022, Vol. 17 Issue 1, p1-18. 18p.

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