Data sets can be generated with primers entirely outside of the IGHV-IGHD-IGHV-encoded sequence but also by using primers within e.g. FR1, e.g. Biomed2. How will different annotation tools address challenges with shorter reads that will cause increased numbers of ambiguous calls?
Data sets can be generated with primers entirely outside of the IGHV-IGHD-IGHV-encoded sequence but also by using primers within e.g. FR1, e.g. Biomed2. How will different annotation tools address challenges with shorter reads that will cause increased numbers of ambiguous calls?