algo-basic-algorithms

name	algo-basic-algorithms
description	Compute GCD/LCM via Euclid's algorithm, find roots with Newton's method, and count k-mers using dict/Counter vs O(n^2) list-scan. Use for GCD/LCM math, root-finding, k-mer counting, or Big-O complexity questions.
tool_type	python
primary_tool	Python

Basic Algorithms

When to Use

• Computing GCD/LCM for fraction simplification, modular arithmetic, or RSA key generation.
• Finding cube roots (or other roots) numerically via Newton-Raphson iteration.
• Counting k-mers in a DNA/RNA sequence and need to justify why a hash map beats a list scan.
• Explaining/verifying Big-O complexity of a nested-loop bioinformatics routine (e.g., all-vs-all pairwise distance) before it is run at genome scale.
• Teaching or reviewing foundational CS algorithms (sorting, ciphers) as building blocks for larger pipelines.

Version Compatibility

Pure Python stdlib — no third-party dependencies. Works on Python ≥3.9 (uses list[str] / dict[str, int] builtin generics).

Prerequisites

• Python ≥3.9. No packages to install.
• Familiarity with Big-O notation (see ## Complexity Table below for concrete numbers).

Complexity Table

Algorithm	Best	Average	Worst	Space
Euclidean GCD	O(1)	O(log min(a,b))	O(log min(a,b))	O(1)
Newton's cube root	O(1)	O(log 1/ε)	O(max_iter)	O(1)
k-mer counting (dict)	O(n·k)	O(n·k)	O(n·k)	O(n)
k-mer counting (list scan)	O(n·k)	O(n²·k)	O(n²·k)	O(n)

Euclidean GCD / LCM

Goal: compute the greatest common divisor and least common multiple of two integers.

Approach: repeatedly replace (a, b) with (b, a % b) until b == 0; the key identity is gcd(a, b) == gcd(b, a % b).

def gcd(a: int, b: int) -> int:
    """Greatest common divisor via the Euclidean algorithm.

    Complexity: O(log min(a, b)) time, O(1) space.

    >>> gcd(48, 18)
    6
    >>> gcd(-48, 18)
    6
    """
    a, b = abs(a), abs(b)
    while b != 0:
        a, b = b, a % b
    return a


def lcm(a: int, b: int) -> int:
    """Least common multiple, computed from gcd to avoid overflow in
    other languages: (a // gcd(a, b)) * b, not (a * b) // gcd(a, b).
    """
    if a == 0 or b == 0:
        return 0
    g = gcd(a, b)
    return abs(a // g * b)

Worst case is consecutive Fibonacci numbers (e.g., gcd(89, 55)) — each step still reduces the problem by at least half, so it stays O(log min(a, b)).

Newton's Method — Root Finding

Goal: find x such that x**3 == a (cube root), without **(1/3) (which mishandles negative a).

Approach: iterate x_new = (2*x + a/x**2) / 3, derived from x - f(x)/f'(x) for f(x) = x**3 - a. Convergence is quadratic — correct digits roughly double each iteration.

def cube_root(a: float, epsilon: float = 1e-10, max_iterations: int = 1000) -> float:
    """Cube root of a via Newton-Raphson iteration.

    Complexity: O(log(1/epsilon)) iterations due to quadratic convergence.

    >>> round(cube_root(27), 6)
    3.0
    >>> round(cube_root(-8), 6)
    -2.0
    """
    if a == 0:
        return 0.0
    sign = 1 if a > 0 else -1
    a_abs = abs(a)
    x = a_abs / 2 if a_abs > 1 else a_abs  # initial guess
    for _ in range(max_iterations):
        x_new = (2 * x + a_abs / (x * x)) / 3
        if abs(x_new - x) < epsilon:
            return sign * x_new
        x = x_new
    return sign * x

k-mer Counting: Hash Map vs List Scan

Goal: count occurrences of every k-mer in a sequence — the core operation behind genome-size estimation (Jellyfish), error correction, and de Bruijn graph assembly.

Approach: a list-scan implementation looks for an existing (kmer, count) entry by scanning the whole list on every insert — O(n) per lookup, O(n²·k) overall. A dict gives O(1) average lookup, so the same task is O(n·k). This gap is why every real k-mer counter (Jellyfish, KMC, Counter) uses a hash map, not a list.

from collections import Counter


def count_kmers_list(sequence: str, k: int) -> list[tuple[str, int]]:
    """Count k-mers by linear-scanning a list on every insert.

    Complexity: O(n^2 * k) time — n-k+1 k-mers, each insert scans up to
    n-k+1 existing entries and compares k characters.
    """
    counts: list[list] = []  # [kmer, count] pairs
    for i in range(len(sequence) - k + 1):
        kmer = sequence[i:i + k]
        for entry in counts:
            if entry[0] == kmer:
                entry[1] += 1
                break
        else:
            counts.append([kmer, 1])
    return [(kmer, n) for kmer, n in counts]


def count_kmers_dict(sequence: str, k: int) -> dict[str, int]:
    """Count k-mers with a dict (equivalent to collections.Counter).

    Complexity: O(n * k) time — n-k+1 k-mers, O(k) average hash/compare
    per lookup, O(1) amortized dict insert/update.
    """
    counts: dict[str, int] = {}
    for i in ((sequence) - k + ):
        kmer = sequence[i:i + k]
        counts[kmer] = counts.get(kmer, ) + 
     counts


 () -> Counter:
    
     Counter(sequence[i:i + k]  i  ((sequence) - k + ))

Pitfalls

• Euclidean GCD with negatives: always take abs() first; gcd(-48, 18) must return 6, not -6.
• LCM overflow: Python ints are arbitrary precision, but in other languages a * b overflows before dividing — compute (a // gcd(a, b)) * b.
• Newton's method diverges from a bad initial guess: a/2 works well for a > 1; use a itself for 0 < a <= 1; special-case a == 0 since the update divides by x**2.
• Using float epsilon for exact integer algorithms: GCD needs no tolerance — epsilon-based convergence only applies to numerical methods like Newton's.
• List-scan k-mer counting silently works on toy data, then falls over at genome scale: O(n²·k) is fine for a 100 bp read, catastrophic for a chromosome. Default to dict/Counter; only justify a list if k-mer cardinality is tiny and fixed.
• k-mer window off-by-one: valid start indices are range(len(sequence) - k + 1); using range(len(sequence)) reads past the end and raises/truncates silently via slicing.

See Also

• bio-database-access-blast-searches — when O(n²) all-vs-all sequence comparison must be replaced with heuristic search at scale.
• bio-sequence-io-sequence-statistics — sequence-level statistics that often reuse k-mer counting.
• bio-population-genetics-scikit-allel-analysis — downstream use of counting/complexity tradeoffs on large variant matrices.