Low Coverage Depth Nanopore Sequencing is an Alternative to Genomic Microarrays for Detection of Copy Number Variants in the Human Genome

C Silva; J Ferrao; B Marques; S Pedro; Hildeberto Correia; AS Rodrigues; L Vieira

Low Coverage Depth Nanopore Sequencing is an Alternative to Genomic Microarrays for Detection of Copy Number Variants in the Human Genome

C Silva, J Ferrao, B Marques, S Pedro, Hildeberto Correia, AS Rodrigues, L Vieira

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Number of pages	1
Journal	Medicine
Volume	102
Issue number	13
Publication status	Published - 31 Mar 2023

Cite this

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title = "Low Coverage Depth Nanopore Sequencing is an Alternative to Genomic Microarrays for Detection of Copy Number Variants in the Human Genome",

author = "C Silva and J Ferrao and B Marques and S Pedro and Hildeberto Correia and AS Rodrigues and L Vieira",

year = "2023",

month = mar,

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journal = "Medicine",

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T1 - Low Coverage Depth Nanopore Sequencing is an Alternative to Genomic Microarrays for Detection of Copy Number Variants in the Human Genome

AU - Silva, C

AU - Ferrao, J

AU - Marques, B

AU - Pedro, S

AU - Correia, Hildeberto

AU - Rodrigues, AS

AU - Vieira, L

PY - 2023/3/31

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SN - 1464-2662

VL - 102

JO - Medicine

JF - Medicine

IS - 13

ER -

Low Coverage Depth Nanopore Sequencing is an Alternative to Genomic Microarrays for Detection of Copy Number Variants in the Human Genome

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