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Duquette, C.

Publications and source records attributed to Duquette, C..

2 recordsLinked to original sources

GROQ-seq Enables Cross-site Reproducibility for High-Throughput Measurement of Protein Function

High-throughput functional assays are increasingly used to generate large-scale protein function datasets for protein engineering and machine learning applications. However, the utility of such datasets depends on the reproducibility of the underlying measurements. Here we report reproducible, quantitative measurements of protein sequence-to-function data at scale across two facilities. We analyze GROQ-seq (Growth-based Quantitative Sequencing) measurements of three bacterial transcription factors. Independent barcode measurements of the same sequence produce highly consistent functional estimates, demonstrating strong biological reproducibility (across all transcription factors the mean Root Mean Square Deviation [RMSD] {approx} 0.53 and mean Spearman {approx} 0.63). We also compared experiments performed at two facilities using a shared protocol, but with differing levels of automation and system integration. We observe strong agreement between measurements taken at the two sites (mean RMSD {approx} 0.41 and mean Spearman {approx} 0.730). Orthogonal tests further support this agreement: a classifier trained to distinguish data by site performs near random (AUC = 0.559), and top-ranking variants show strong statistical overlap between experiments. Together, these results demonstrate that GROQ-seq enables reproducible, scalable measurement of protein function suitable for large aggregated datasets.

bioengineering↗

Let’s talk about cardiac T1 mapping

BackgroundRecent reports have shown that T1 mapping sequences agree in phantoms, but exhibit significant differences in vivo. To characterize these differences in the heart, one needs to consider the effects of magnetization transfer (MT) and the T2 relaxation time in the most commonly used cardiac T1 mapping sequences (MOLLI, ShMOLLI and SASHA).\n\nMethodsSix explanted pig hearts were scanned weekly over a period of six weeks on a 3T system with the MOLLI, ShMOLLI, SASHA sequences and an inversion recovery sequence as reference. The T1 bias was computed as the difference between MOLLI, ShMOLLI, SASHA and the reference T1 values. We applied robust correlation statistics to assess the relationships between T1, T2 and MT. All data are publicly available at: http://neuropoly.pub/pigHeartsData.\n\nResultsA systematic T1 bias was present for all sequences, with MOLLI and ShMOLLI underestimating T1 and SASHA slightly overestimating T1 compared to the reference. The correlation of T1 bias with T2 was weak and insignificant. However, MT showed significant associations with T1 bias for all sequences. Our analysis is also available at: http://neuropoly.pub/pigHeartsInteractive.\n\nConclusionWe investigated cardiac T1 mapping sequences in a setting that allowed us to explore their accuracy and their dependence on T2 and MT effects. The T2 effects were not significant, and could not explain the T1 bias of MOLLI, ShMOLLI, SASHA with respect to the reference. On the other hand, the T1 biases exhibited a strong correlation with MT. We conclude that inaccuracies in cardiac T1 mapping are primarily due to magnetization transfer.

biophysics↗