bixverse-rs 0.3.5

//! Helpers for multi-file binary file merging. This is used to combine
//! multiple SingleCells experiments on the R side. It enables the user to
//! combine and merge several experiments.

use rayon::prelude::*;
use std::path::Path;
use std::time::Instant;
use thousands::Separable;

use crate::prelude::*;
use crate::single_cell::sc_data::data_io::CellGeneSparseWriter;

////////////
// Consts //
////////////

/// Number of cells to merge in one go per batch
const MERGE_CELL_BATCH_SIZE: usize = 10_000;

////////////////
// Structures //
////////////////

/// A single input source for the merge operation
#[derive(Debug, Clone)]
pub struct BinMergeTask {
    /// Identifier for this experiment, becomes a column in obs.
    pub exp_id: String,
    /// Path to the input cells .bin file.
    pub bin_cells_path: String,
    /// 0-indexed original cell indices to include from this input (typically
    /// the cells with `to_keep = TRUE` in the input's obs).
    pub cells_to_keep: Vec<usize>,
    /// Vector indexed by the input's local gene index. `Some(universe_idx)` if
    /// the gene survives the intersection, `None` if it does not.
    pub gene_local_to_universe: Vec<Option<u32>>,
}

/// Per-file output of the merge
///
/// ### Notes
///
/// `lib_size` semantics depend on `renormalise`:
/// - `renormalise = false`: the original library size from the input bin
///   (i.e. sum over the input's gene set, pre-intersection).
/// - `renormalise = true`: recomputed sum over the surviving (intersected)
///   gene set.
#[derive(Debug, Clone)]
pub struct PerFileMergeResult {
    /// Experiment id string
    pub exp_id: String,
    /// The library size per cell per file
    pub lib_size: Vec<usize>,
    /// The number with non-zero expression genes per cells
    pub nnz: Vec<usize>,
}

/// Total result of merging multiple SingleCells bin files
#[derive(Debug, Clone)]
pub struct MultiSingleCellsResult {
    /// The total number of cells across the experiments
    pub total_cells: usize,
    /// The total number of genes across the experiments
    pub total_genes: usize,
    /// A vectors of [PerFileMergeResult]
    pub per_file: Vec<PerFileMergeResult>,
}

/////////////
// Helpers //
/////////////

/// Remap a single cell onto the universe gene indexing
///
/// Surviving entries are sorted by universe index so the resulting chunk has
/// indices in ascending order, matching the invariant of the rest of the
/// pipeline.
///
/// ### Params
///
/// * `cell` - Reference to the [CsrCellChunk]
/// * `gene_local_to_universe` - The mapping between the local genes to the
///   universe.
/// * `new_cell_idx` - New cell index
/// * `renormalise` - Renormalise the counts.
/// * `target_size` - The target size to normalise to
///
/// ### Returns
///
/// The new chunk plus `(library_size, nnz)` for reporting.
fn remap_cell(
    cell: &CsrCellChunk,
    gene_local_to_universe: &[Option<u32>],
    new_cell_idx: usize,
    renormalise: bool,
    target_size: f32,
) -> (CsrCellChunk, usize, usize) {
    let mut entries: Vec<(u32, u32, F16)> = Vec::with_capacity(cell.indices.len());
    for (i, &local_idx) in cell.indices.iter().enumerate() {
        if let Some(universe_idx) = gene_local_to_universe[local_idx as usize] {
            entries.push((universe_idx, cell.data_raw.get(i), cell.data_norm[i]));
        }
    }
    entries.sort_unstable_by_key(|&(u, _, _)| u);

    let nnz = entries.len();

    if renormalise {
        let raw: Vec<u32> = entries.iter().map(|&(_, r, _)| r).collect();
        let indices: Vec<u32> = entries.iter().map(|&(u, _, _)| u).collect();
        let new_chunk = CsrCellChunk::from_data(&raw, &indices, new_cell_idx, target_size, true);
        let lib_size = new_chunk.library_size;
        (new_chunk, lib_size, nnz)
    } else {
        let raw: Vec<u32> = entries.iter().map(|&(_, r, _)| r).collect();
        let norm: Vec<F16> = entries.iter().map(|&(_, _, n)| n).collect();
        let indices: Vec<u32> = entries.iter().map(|&(u, _, _)| u).collect();
        let new_chunk = CsrCellChunk {
            data_raw: RawCounts::from_u32_auto(&raw),
            data_norm: norm,
            library_size: cell.library_size,
            indices,
            original_index: new_cell_idx,
            to_keep: true,
        };
        (new_chunk, cell.library_size, nnz)
    }
}

//////////
// Main //
//////////

/// Merge multiple existing bin files into a single new cells .bin file
///
/// Streams cells from each input bin, remaps gene indices onto the
/// intersection universe, and writes a unified cell-based output. The
/// gene-based companion file must be generated separately afterwards via
/// `generate_gene_based_data_streaming`.
///
/// ### Params
///
/// * `tasks` - One `BinMergeTask` per input source.
/// * `output_bin_path` - Path to the new cells .bin file to write.
/// * `universe_size` - Number of genes in the intersection universe.
/// * `renormalise` - If `true`, recompute `data_norm` against `target_size`
///   using each cell's surviving raw counts. If `false`, pass `data_norm`
///   through untouched; the caller is responsible for ensuring all inputs
///   were normalised against the same `target_size`.
/// * `target_size` - Target library size for renormalisation. Ignored when
///   `renormalise = false`.
/// * `verbose` - Controls verbosity.
///
/// ### Returns
///
/// `MultiSingleCellsResult` summarising the merge.
pub fn merge_sc_bin_files<P: AsRef<Path>>(
    tasks: &[BinMergeTask],
    output_bin_path: P,
    universe_size: usize,
    renormalise: bool,
    target_size: f32,
    verbose: bool,
) -> Result<MultiSingleCellsResult, BixverseErrors> {
    let total_cells: usize = tasks.iter().map(|t| t.cells_to_keep.len()).sum();

    let start = Instant::now();

    if verbose {
        println!(
            "Merging {} input files, {} total cells, {} universe genes (renormalise = {})",
            tasks.len(),
            total_cells.separate_with_underscores(),
            universe_size.separate_with_underscores(),
            renormalise
        );
    }

    let mut writer = CellGeneSparseWriter::new(output_bin_path, true, total_cells, universe_size)?;

    let mut per_file: Vec<PerFileMergeResult> = Vec::with_capacity(tasks.len());
    let mut new_cell_idx: usize = 0;

    for (task_idx, task) in tasks.iter().enumerate() {
        if verbose {
            println!(
                "  Input {}/{} ({}): {} cells",
                task_idx + 1,
                tasks.len(),
                task.exp_id,
                task.cells_to_keep.len().separate_with_underscores()
            );
        }

        let reader = ParallelSparseReader::new(&task.bin_cells_path)?;

        let mut lib_size_out: Vec<usize> = Vec::with_capacity(task.cells_to_keep.len());
        let mut nnz_out: Vec<usize> = Vec::with_capacity(task.cells_to_keep.len());

        for batch in task.cells_to_keep.chunks(MERGE_CELL_BATCH_SIZE) {
            let cells = reader.read_cells_parallel(batch)?;

            let remapped: Vec<(CsrCellChunk, usize, usize)> = cells
                .par_iter()
                .enumerate()
                .map(|(offset, cell)| {
                    let idx = new_cell_idx + offset;
                    remap_cell(
                        cell,
                        &task.gene_local_to_universe,
                        idx,
                        renormalise,
                        target_size,
                    )
                })
                .collect();

            for (chunk, lib_size_i, nnz_i) in remapped {
                lib_size_out.push(lib_size_i);
                nnz_out.push(nnz_i);
                writer.write_cell_chunk(chunk)?;
            }

            new_cell_idx += batch.len();
        }

        per_file.push(PerFileMergeResult {
            exp_id: task.exp_id.clone(),
            lib_size: lib_size_out,
            nnz: nnz_out,
        });

        if verbose {
            println!("   Task done in {:.2?}", start.elapsed());
        }
    }

    writer.finalise()?;

    if verbose {
        println!(
            "Merge complete: {} cells written in {:.2?}",
            total_cells.separate_with_underscores(),
            start.elapsed()
        );
    }

    Ok(MultiSingleCellsResult {
        total_cells,
        total_genes: universe_size,
        per_file,
    })
}