48 research outputs found
Carbon-Efficient Neural Architecture Search
This work presents a novel approach to neural architecture search (NAS) that
aims to reduce energy costs and increase carbon efficiency during the model
design process. The proposed framework, called carbon-efficient NAS (CE-NAS),
consists of NAS evaluation algorithms with different energy requirements, a
multi-objective optimizer, and a heuristic GPU allocation strategy. CE-NAS
dynamically balances energy-efficient sampling and energy-consuming evaluation
tasks based on current carbon emissions. Using a recent NAS benchmark dataset
and two carbon traces, our trace-driven simulations demonstrate that CE-NAS
achieves better carbon and search efficiency than the three baselines
Neural Architecture Search using Deep Neural Networks and Monte Carlo Tree Search
Neural Architecture Search (NAS) has shown great success in automating the
design of neural networks, but the prohibitive amount of computations behind
current NAS methods requires further investigations in improving the sample
efficiency and the network evaluation cost to get better results in a shorter
time. In this paper, we present a novel scalable Monte Carlo Tree Search (MCTS)
based NAS agent, named AlphaX, to tackle these two aspects. AlphaX improves the
search efficiency by adaptively balancing the exploration and exploitation at
the state level, and by a Meta-Deep Neural Network (DNN) to predict network
accuracies for biasing the search toward a promising region. To amortize the
network evaluation cost, AlphaX accelerates MCTS rollouts with a distributed
design and reduces the number of epochs in evaluating a network by transfer
learning, which is guided with the tree structure in MCTS. In 12 GPU days and
1000 samples, AlphaX found an architecture that reaches 97.84\% top-1 accuracy
on CIFAR-10, and 75.5\% top-1 accuracy on ImageNet, exceeding SOTA NAS methods
in both the accuracy and sampling efficiency. Particularly, we also evaluate
AlphaX on NASBench-101, a large scale NAS dataset; AlphaX is 3x and 2.8x more
sample efficient than Random Search and Regularized Evolution in finding the
global optimum. Finally, we show the searched architecture improves a variety
of vision applications from Neural Style Transfer, to Image Captioning and
Object Detection.Comment: To appear in the Thirty-Fourth AAAI conference on Artificial
Intelligence (AAAI-2020
Separating Invisible Sounds Toward Universal Audiovisual Scene-Aware Sound Separation
The audio-visual sound separation field assumes visible sources in videos,
but this excludes invisible sounds beyond the camera's view. Current methods
struggle with such sounds lacking visible cues. This paper introduces a novel
"Audio-Visual Scene-Aware Separation" (AVSA-Sep) framework. It includes a
semantic parser for visible and invisible sounds and a separator for
scene-informed separation. AVSA-Sep successfully separates both sound types,
with joint training and cross-modal alignment enhancing effectiveness.Comment: Accepted at ICCV 2023 - AV4D, 4 figures, 3 table
Toward more accurate variant calling for “personal genomes”
To date, researchers and clinicians use widely different methods for detecting and reporting human genetic variation. As the size of academic and private databases grow and as the use of the existing genomic techniques expand, researchers and clinicians stand to greatly benefit from the standardization of data generating approaches and analysis methodologies. To successfully implement genomic analyses in the clinic, it will be critically important to optimize the existing pipelines for attaining a higher sensitivity and specificity for more accurate and consistent variant calling
Low concordance of multiple variant-calling pipelines: practical implications for exome and genome sequencing
BACKGROUND: To facilitate the clinical implementation of genomic medicine by next-generation sequencing, it will be critically important to obtain accurate and consistent variant calls on personal genomes. Multiple software tools for variant calling are available, but it is unclear how comparable these tools are or what their relative merits in real-world scenarios might be. METHODS: We sequenced 15 exomes from four families using commercial kits (Illumina HiSeq 2000 platform and Agilent SureSelect version 2 capture kit), with approximately 120X mean coverage. We analyzed the raw data using near-default parameters with five different alignment and variant-calling pipelines (SOAP, BWA-GATK, BWA-SNVer, GNUMAP, and BWA-SAMtools). We additionally sequenced a single whole genome using the sequencing and analysis pipeline from Complete Genomics (CG), with 95% of the exome region being covered by 20 or more reads per base. Finally, we validated 919 single-nucleotide variations (SNVs) and 841 insertions and deletions (indels), including similar fractions of GATK-only, SOAP-only, and shared calls, on the MiSeq platform by amplicon sequencing with approximately 5000X mean coverage. RESULTS: SNV concordance between five Illumina pipelines across all 15 exomes was 57.4%, while 0.5 to 5.1% of variants were called as unique to each pipeline. Indel concordance was only 26.8% between three indel-calling pipelines, even after left-normalizing and intervalizing genomic coordinates by 20 base pairs. There were 11% of CG variants falling within targeted regions in exome sequencing that were not called by any of the Illumina-based exome analysis pipelines. Based on targeted amplicon sequencing on the MiSeq platform, 97.1%, 60.2%, and 99.1% of the GATK-only, SOAP-only and shared SNVs could be validated, but only 54.0%, 44.6%, and 78.1% of the GATK-only, SOAP-only and shared indels could be validated. Additionally, our analysis of two families (one with four individuals and the other with seven), demonstrated additional accuracy gained in variant discovery by having access to genetic data from a multi-generational family. CONCLUSIONS: Our results suggest that more caution should be exercised in genomic medicine settings when analyzing individual genomes, including interpreting positive and negative findings with scrutiny, especially for indels. We advocate for renewed collection and sequencing of multi-generational families to increase the overall accuracy of whole genomes
Abnormal bile acid metabolism is an important feature of gut microbiota and fecal metabolites in patients with slow transit constipation
Destructions in the intestinal ecosystem are implicated with changes in slow transit constipation (STC), which is a kind of intractable constipation characterized by colonic motility disorder. In order to deepen the understanding of the structure of the STC gut microbiota and the relationship between the gut microbiota and fecal metabolites, we first used 16S rRNA amplicon sequencing to evaluate the gut microbiota in 30 STC patients and 30 healthy subjects. The α-diversity of the STC group was changed to a certain degree, and the β-diversity was significantly different, which indicated that the composition of the gut microbiota of STC patients was inconsistent with healthy subjects. Among them, Bacteroides, Parabacteroides, Desulfovibrionaceae, and Ruminiclostridium were significantly upregulated, while Subdoligranulum was significantly downregulated. The metabolomics showed that different metabolites between the STC and the control group were involved in the process of bile acids and lipid metabolism, including taurocholate, taurochenodeoxycholate, taurine, deoxycholic acid, cyclohexylsulfamate, cholic acid, chenodeoxycholate, arachidonic acid, and 4-pyridoxic acid. We found that the colon histomorphology of STC patients was significantly disrupted, and TGR5 and FXR were significantly downregulated. The differences in metabolites were related to changes in the abundance of specific bacteria and patients’ intestinal dysfunction. Analysis of the fecal genomics and metabolomics enabled separation of the STC from controls based on random forest model prediction [STC vs. control (14 gut microbiota and metabolite biomarkers)—Sensitivity: 1, Specificity: 0.877]. This study provided a perspective for the diagnosis and intervention of STC related with abnormal bile acid metabolism
Role of gut microbiota regulation in traditional Chinese medicine treatment of non-alcoholic fatty liver disease
Based on recent studies which have shown that gut microbiota plays an important role in the pathogenesis of non-alcoholic fatty liver disease (NAFLD), the article elaborates on the relationship of NAFLD with intestinal endotoxemia, short-chain fatty acids, bile acid metabolism, and endogenous ethanol. By illustrating the author′s research progress in the relationship between traditional Chinese medicine (TCM) regulation of gut microbiota and NAFLD treatment, the article proposes that this approach is not only a clinical practice of TCM in the modern era, it may also become a new strategy in the treatment of NAFLD