Update projects.tmp

Author: visze

templates/projects.tmp

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            <a href="https://cadd.bihealth.org/">CADD</a> - Combined Annotation Dependent Depletion (CADD) framework to score the deleteriousness of single nucleotide variants, multi-allelic substitutions and short insertion/deletions in the human genome (GRCh37/38).
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            <a href="https://github.com/kircherlab/CADD-scripts">CADD scripts</a> - Offline tool to score the deleteriousness of single nucleotide variants, multi-allelic substitutions and short insertion/deletions in the human genome in an on-site installation.
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+           <a href="https://cadd-threshold.kircherlab.bihealth.org">CADD-ThresholdApp</a> - Visualization of ClinVar variants distributed across CADD PHRED-score thresholds to help choose sensible score cut-offs for specific use cases.
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             <a href="https://cadd-sv.bihealth.org/">CADD-SV</a> - CADD-SV is a framework to estimate the impact of Structural Variants (SVs) in the human genome. We combine various annotations to predict the deleteriousness of human deletions. We provide a webserver for easy scoring and download of pre-scored SVs.