Tiffanie Godelaine, Maxime Zanella, Karim El Khoury +2cs.CV cs.AI
Automating the analysis of whole-slide images has high clinical value, since characterizing cancers requires examining them in detail. Such analysis increasingly relies on vision-language models that provide patch-level zero-shot predictions. However, these predictions remain noisy and must be refined with a few annotations. A promising paradigm for this refinement is few-shot transduction. Rather than treating each patch independently, these methods leverage the relations between patches, together with a few annotations, to refine all predictions jointly. However, current transductive methods are evaluated under conditions that overlook key properties of whole-slide images: (i) datasets consist of independent patches extracted from multiple slides, ignoring the complex tissue organization; (ii) datasets are mostly balanced, whereas a single whole-slide image exhibits severe class imbalance, with several classes absent; and (iii) annotations are sampled at random, without reflecting how a pathologist annotates a limited number of regions. To align the transduction paradigm to realistic whole-slide settings, we introduce the following contributions. First, we propose SlideCRF, which adapts conditional random fields for whole-slide images by combining spatial and biological cues while accounting for classes that may be absent from a given slide. Second, we provide a set of realistic annotation protocols, based on spatially localized clicks and scribbles, modeling different pathologist interactions, such as the iterative correction of model errors. Across four datasets, we show that SlideCRF outperforms current transductive methods in macro F1, improving over the zero-shot predictions by +24.2% and +37.5% with one and 16 clicks per present class, respectively.
Conversational speech emotion recognition must reconcile acoustic evidence across temporal scales with two interaction processes: cross-speaker contextual influence and within-speaker emotion evolution. We propose DSSM-CRF, an audio-only architecture that explicitly separates these processes. Bidirectional state-space models encode fused self-supervised speech representations at frame and dialogue scales, so each utterance representation captures local prosody and context from all speakers. The decoder then orders each speaker's utterances into an independent dynamic conditional random field chain. Consecutive utterances in a speaker's chain form a transition pair whose score combines a corpus-level transition matrix with a residual predicted from the two contextualized utterances. An auxiliary objective supervises whether each pair changes emotion but does not participate in Viterbi inference. Thus, interlocutor turns affect contextual emotion scores without being treated as transitions in another speaker's emotion trajectory. DSSM-CRF achieves 75.81% UA and 74.90% WA on IEMOCAP, and 54.72% WA and 49.31% WF1 on MELD. Matched controls demonstrate complementary gains from speaker-wise factorization and CRF modeling.
Nicolas Floquet, Joseph Le Roux, Nadi Tomehcs.CL cs.LG
Sequence labelling, a core task of Natural Language Processing (NLP), consists in assigning each token of an input sentence a label. From a Machine Learning point of view, sequence labelling is often cast as a Linear-Chain Conditional Random Field (CRF) parametrised by a neural network. While this approach gives good empirical results, CRFs assume a finite decision span (eg label bigrams) which can limit their expressivity and hurt performance when long-range dependencies are required. We show we can leverage diffusion to train a CRF conditioned on an entire label sequence, with the caveat that the condition is on a noisy version of labels. We show experimentally that this method, in conjunction with approximate CRF inference, improves label accuracy with a 16.5% error reduction for POS-tagging.