Papers: 10.1038/s41598-021-85182-w

https://doi.org/10.1038/s41598-021-85182-w

Sanger sequencing is no longer always necessary based on a single-center validation of 1109 NGS variants in 825 clinical exomes

Cited by: 30
Author(s): Ana Arteche‐López, Almudena Ávila-Fernández, Raquel Escutia Romero, Rosa Riveiro-Álvarez, Miguel Ángel López-Martínez, A Giménez-Pardo, Camilo Vélez-Monsalve, J. Gallego-Merlo, I García-Vara, Berta Almoguera, Ana Bustamante-Aragonés, Fiona Blanco‐Kelly, Saoud Tahsin-Swafiri, Elvira Rodríguez‐Pinilla, Pablo Mínguez, Isabel Lorda, María José Trujillo-Tiebas, Carmen Ayuso
Published: over 5 years ago

Software Mentions 1

pypi: alignment
Native Python library for generic sequence alignment.
Papers that mentioned: 30
Very Likely Science (65)