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Academic Journal

High incidence of AZF duplications in clan-structured Iranian populations detected through Y chromosome sequencing read depth analysis.

Authors : Hajiesmaeil, Mogge¹ (AUTHOR); Ravasini, Francesco¹ (AUTHOR); Risi, Flavia¹ (AUTHOR)

Source: Scientific Reports. 7/22/2023, Vol. 13 Issue 1, p1-9. 9p.

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Towards mouse genetic-specific RNA-sequencing read mapping.

Authors : Gobet, Nastassia^1,2 (AUTHOR); Jan, Maxime^1,3 (AUTHOR); Franken, Paul¹ (AUTHOR)

Source: PLoS Computational Biology. 9/26/2022, Vol. 18 Issue 9, p1-17. 17p. 1 Chart, 4 Graphs.

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CONY: A Bayesian procedure for detecting copy number variations from sequencing read depths.

Authors : Wei, Yu-Chung¹; Huang, Guan-Hua²

Source: Scientific Reports. 6/26/2020, Vol. 10 Issue 1, p1-14. 14p.

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Late Diagnosis of 18p Syndrome with Movement Disorders by Whole Exome Sequencing Read‐Depth Based Algorithm.

Authors : Mouraux, Charlotte¹ (AUTHOR) ; Depierreux, Frédérique^1,2 (AUTHOR)

Source: Movement Disorders Clinical Practice. Oct2023, Vol. 10 Issue 10, p1557-1558. 2p.

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De novo genome assembly and annotation of Australia's largest freshwater fish, the Murray cod (Maccullochella peelii), from Illumina and Nanopore sequencing read.

Authors : Austin, Christopher M.^1,2,3; Mun Hua Tan^1,2,3; Harrisson, Katherine A.⁴

Source: GigaScience. Aug2017, Vol. 6 Issue 8, p1-6. 6p.

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Filtration and Normalization of Sequencing Read Data in Whole-Metagenome Shotgun Samples.

Authors : Chouvarine, Philippe¹ ; Wiehlmann, Lutz^2,3; Moran Losada, Patricia²

Source: PLoS ONE. 10/19/2016, Vol. 11 Issue 10, p1-16. 16p.

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BamView: visualizing and interpretation of next-generation sequencing read alignments.

Authors : Carver, Tim; Harris, Simon R.; Otto, Thomas D.

Source: Briefings in Bioinformatics. Mar2013, Vol. 14 Issue 2, p203-212. 10p. 3 Color Photographs, 1 Black and White Photograph, 1 Diagram, 2 Charts.

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Copy number variation detection using next generation sequencing read counts.

Authors : Heng Wang^1,2,3 ; Nettleton, Dan⁴ ; Kai Ying⁵

Source: BMC Bioinformatics. 2014, Vol. 15 Issue 1, p2-27. 26p. 1 Diagram, 7 Charts, 4 Graphs.

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RNA sequencing read depth requirement for optimal transcriptome coverage in Hevea brasiliensis.

Authors : Keng-See Chow¹ ; Ghazali, Ahmad-Kamal² ; Chee-Choong Hoh²

Source: BMC Research Notes. 2014, Vol. 7 Issue 1, p1-25. 25p. 2 Diagrams, 5 Charts, 2 Graphs.

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Detection of copy number variation from array intensity and sequencing read depth using a stepwise Bayesian model.

Authors : Zhang, Zhengdong D.¹ ; Gerstein, Mark B.^2,3,4

Source: BMC Bioinformatics. 2010, Vol. 11, p539-551. 13p.

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فلترة النتائج

High incidence of AZF duplications in clan-structured Iranian populations detected through Y chromosome sequencing read depth analysis.

Towards mouse genetic-specific RNA-sequencing read mapping.

CONY: A Bayesian procedure for detecting copy number variations from sequencing read depths.

Late Diagnosis of 18p Syndrome with Movement Disorders by Whole Exome Sequencing Read‐Depth Based Algorithm.

De novo genome assembly and annotation of Australia's largest freshwater fish, the Murray cod (Maccullochella peelii), from Illumina and Nanopore sequencing read.

Filtration and Normalization of Sequencing Read Data in Whole-Metagenome Shotgun Samples.

BamView: visualizing and interpretation of next-generation sequencing read alignments.

Copy number variation detection using next generation sequencing read counts.

RNA sequencing read depth requirement for optimal transcriptome coverage in Hevea brasiliensis.

Detection of copy number variation from array intensity and sequencing read depth using a stepwise Bayesian model.

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