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0
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ClairS: a deep-learning method for long-read tumor-normal pair somatic small variant calling.
(nature.com)
|
Zheng Z
…
Luo R
Nature Methods
2026-07-01
|
#sequencing
#variants
#somatic
#cancer
#deep learning
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0
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Benchmarking of real-time, field-deployable whole-genome sequencing of Plasmodium falciparum using Nanopore technology.
(microbiologyresearch.org)
|
Razook Z
…
Barry AE
Microbial Genomics
2026-07-01
|
#malaria
#sequencing
#genomics
#parasite
#variants
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0
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Likelihood-based optimization enables accurate copy number estimation for paralogous genes using exome data.
(academic.oup.com)
|
Byun SY
…
Bansal V
Bioinformatics
2026-07-01
|
#sequencing
#exome
#copy_number_variation
#variants
#computational methods
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0
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Complement Gene Variants Define the Conformational Dynamics of C3 Convertase.
(onlinelibrary.wiley.com)
|
Martin Merinero H
…
Zhang Y
European Journal of Immunology
2026-07-01
|
#complement
#immunity
#variants
#genetics
#protein-interactions
|