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Sequencing analysis

Assess ER folding regulation in the MCF7 treatment experiment

TranscriptomicsProtein foldingDeterministic
20261012t185947z-campaign-594b77e9/mcf7-er-discovery
Recorded score0.0%Task-specific rubric
EvaluationRecorded runSaved files
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# Assess ER folding regulation in the MCF7 treatment experiment

The lab wants to know whether its 24-hour MCF7 E2 comparison supports preferential transcriptional regulation of a specific protein-folding process in the endoplasmic reticulum (ER). Use all four supplied PRO-seq read sets and the authentic experimental, genome and biochemical records. Identify the specific ER folding process containing the strongest relative reduction in a member’s transcription, among the ER folding proteins described in the supplied sources. Decide whether the labelled libraries support a common decrease of that process relative to the other source-described ER folding proteins. Seek evidence that challenges your decision. Include only proteins with their own folding-role descriptions; exclude roles restricted to another tissue. Complete only findings.json. This decision concerns relative nascent transcription in the supplied libraries, not protein activity or population significance.

How was it graded?

Code compares submitted answer fields with reference values. Written reasoning is not graded.

Fraction of criteria passed; every criterion has weight one.

LLM judge: None — deterministic grading

Task files

Choose an evidence file.

Grading criteria

2 of 2 criteria
C-001failCritical
Identify the process containing the strongest relative transcriptional reduction

Earns credit

In findings.json, result_genes must contain exactly CANX, CALR and PDIA3 (ENSG00000127022, ENSG00000179218, ENSG00000167004), the source-described members of the calnexin/calreticulin folding cycle. This identifies the process containing the strongest relative transcriptional reduction; it does not claim that every member decreases together.

Does not earn credit

No credit if a required gene is omitted, an extra gene is included, a gene is repeated (including under an alias), or result_genes is missing or is not a list of strings.

Accepted alternatives

Gene order does not matter. Use the listed Ensembl IDs, their versioned IDs from the supplied annotation, or the symbols CANX, CALR and PDIA3. Equivalent IDs and symbols may be mixed; each gene must appear exactly once.

Weight: 1

Input evidence




Entire supplied 8,000,000-record FASTQ, both source lanes. · Exact nascent-RNA observations for the labelled library; no computed results are supplied.
TSV lines 1–5: header and Arpeggio IDs 1045–1048; 24hr, treatment IDs, replicate labels and PRO assay. · Maps libraries to the actual experiment.
TSV lines 1–3: header and treatment IDs 275/282, DMSO/E2 descriptions. · DMSO/E2 identities; unresolved dose does not change labelled-library comparison.
Header and exact rows: ENSG00000127022.16 CANX chr5:179678627-179731641 +; ENSG00000204389.10 HSPA1A chr6:31815542-31817946 +; ENSG00000044574.9 HSPA5 chr9:125234852-125241382 -; ENSG00000149428.21 HYOU1 chr11:119044187-119057227 -; ENSG00000166598.16 HSP90B1 chr12:103930106-103953931 +; ENSG00000080824.19 HSP90AA1 chr14:102080741-102139699 -; ENSG00000167004.14 PDIA3 chr15:43746393-43773279 +; ENSG00000179218.15 CALR chr19:12938577-12944489 + · Maps source identities to the supplied GRCh38/GENCODE v44 annotation.
Exact BED6 rows, zero-based half-open spans: ENSG00000127022.16 CANX chr5:179678627-179731641 +; ENSG00000204389.10 HSPA1A chr6:31815542-31817946 +; ENSG00000044574.9 HSPA5 chr9:125234852-125241382 -; ENSG00000149428.21 HYOU1 chr11:119044187-119057227 -; ENSG00000166598.16 HSP90B1 chr12:103930106-103953931 +; ENSG00000080824.19 HSP90AA1 chr14:102080741-102139699 -; ENSG00000167004.14 PDIA3 chr15:43746393-43773279 +; ENSG00000179218.15 CALR chr19:12938577-12944489 + · Authentic zero-based half-open gene spans and genomic strands.
Protocol excerpt, active polymerases, nascent RNA and sequencing from the 3-prime end. · Makes the assayed quantity and strand attribution discoverable.
BiP is called an ER chaperone and is described binding unfolded proteins. · Authentic source text establishes membership and function, not an experimental outcome.
Expression of BiP/GRP78/HSPA5: alias identity. · Authentic source text establishes membership and function, not an experimental outcome.
GN and FUNCTION: HSP90B1 processing and folding roles in the ER. · Authentic source text establishes membership and function, not an experimental outcome.
Summary: HYOU1 folding/secretion in the ER and alternate-localization caveat. · Authentic source text establishes membership and function, not an experimental outcome.
Description: CANX/CALR lectins and their named folding cycle; CLGN tissue restriction. · Authentic source text establishes membership and function, not an experimental outcome.
PDIA3 compartment, aliases and annotated ERp57 binding within that cycle. · Authentic source text establishes membership and function, not an experimental outcome.
GN, FUNCTION and SUBCELLULAR LOCATION: comparison folding role and locations. · Authentic source text establishes membership and function, not an experimental outcome.
Summary: HSPA1A folding in cytosol/organelles and related-gene cluster. · Authentic source text establishes membership and function, not an experimental outcome.

Reference evidence

computed-reference · computed-reference.gold/local.policies.*.er_log_share_changes and attempt2_final_endpoints; final-selection-independent-check.json documents all supported rankings
Exact supplied-read reference and independent coverage/count arithmetic support the selected cycle and reject coordinated decrease. Diagnostic contrast is private and is not required in the answer.

Recorded result / GPT 6.1 sol

Failed. result_genes: matched 2 of 3 reference members. Missing: PDIA3.

result_genes
result_genes
C-001
C-003failCritical
Reject unsupported coordinated functional decrease

Earns credit

In findings.json, decision must be the JSON boolean false. The labelled-library evidence does not support a common decrease of this folding process relative to the other source-described ER folding proteins. The claim concerns relative nascent transcription, not protein activity or population significance.

Does not earn credit

No credit for true, a missing value, null, a number, or a string such as "false". The grader requires the boolean false.

Weight: 1

Input evidence




Entire supplied 8,000,000-record FASTQ, both source lanes. · Exact nascent-RNA observations for the labelled library; no computed results are supplied.
TSV lines 1–5: header and Arpeggio IDs 1045–1048; 24hr, treatment IDs, replicate labels and PRO assay. · Maps libraries to the actual experiment.
TSV lines 1–3: header and treatment IDs 275/282, DMSO/E2 descriptions. · DMSO/E2 identities; unresolved dose does not change labelled-library comparison.
Header and exact rows: ENSG00000127022.16 CANX chr5:179678627-179731641 +; ENSG00000204389.10 HSPA1A chr6:31815542-31817946 +; ENSG00000044574.9 HSPA5 chr9:125234852-125241382 -; ENSG00000149428.21 HYOU1 chr11:119044187-119057227 -; ENSG00000166598.16 HSP90B1 chr12:103930106-103953931 +; ENSG00000080824.19 HSP90AA1 chr14:102080741-102139699 -; ENSG00000167004.14 PDIA3 chr15:43746393-43773279 +; ENSG00000179218.15 CALR chr19:12938577-12944489 + · Maps source identities to the supplied GRCh38/GENCODE v44 annotation.
Exact BED6 rows, zero-based half-open spans: ENSG00000127022.16 CANX chr5:179678627-179731641 +; ENSG00000204389.10 HSPA1A chr6:31815542-31817946 +; ENSG00000044574.9 HSPA5 chr9:125234852-125241382 -; ENSG00000149428.21 HYOU1 chr11:119044187-119057227 -; ENSG00000166598.16 HSP90B1 chr12:103930106-103953931 +; ENSG00000080824.19 HSP90AA1 chr14:102080741-102139699 -; ENSG00000167004.14 PDIA3 chr15:43746393-43773279 +; ENSG00000179218.15 CALR chr19:12938577-12944489 + · Authentic zero-based half-open gene spans and genomic strands.
Protocol excerpt, active polymerases, nascent RNA and sequencing from the 3-prime end. · Makes the assayed quantity and strand attribution discoverable.
BiP is called an ER chaperone and is described binding unfolded proteins. · Authentic source text establishes membership and function, not an experimental outcome.
Expression of BiP/GRP78/HSPA5: alias identity. · Authentic source text establishes membership and function, not an experimental outcome.
GN and FUNCTION: HSP90B1 processing and folding roles in the ER. · Authentic source text establishes membership and function, not an experimental outcome.
Summary: HYOU1 folding/secretion in the ER and alternate-localization caveat. · Authentic source text establishes membership and function, not an experimental outcome.
Description: CANX/CALR lectins and their named folding cycle; CLGN tissue restriction. · Authentic source text establishes membership and function, not an experimental outcome.
PDIA3 compartment, aliases and annotated ERp57 binding within that cycle. · Authentic source text establishes membership and function, not an experimental outcome.
GN, FUNCTION and SUBCELLULAR LOCATION: comparison folding role and locations. · Authentic source text establishes membership and function, not an experimental outcome.
Summary: HSPA1A folding in cytosol/organelles and related-gene cluster. · Authentic source text establishes membership and function, not an experimental outcome.

Reference evidence

computed-reference · computed-reference.gold/local.policies.*.er_log_share_changes and attempt2_final_endpoints; final-selection-independent-check.json documents all supported rankings
Exact supplied-read reference and independent coverage/count arithmetic support the selected cycle and reject coordinated decrease. Diagnostic contrast is private and is not required in the answer.

Recorded result / GPT 6.1 sol

Failed. Submitted decision = true; required the JSON boolean false.

decision
decision
C-003